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Earnings Call: Q3 2022

Oct 19, 2022

Operator

Good morning, and thank you for standing by. Welcome to Abbott's third quarter 2022 earnings conference call. All participants will be able to listen only until the question-and-answer portion of this call. During the question-and-answer session, you will be able to ask your question by pressing the star one one keys on your touchtone phone. This call is being recorded by Abbott. With the exception of any participant's questions asked during the question-and-answer session, the entire call, including the question-and-answer session, is material copyrighted by Abbott. It cannot be recorded or rebroadcast without Abbott's express written permission. I would now like to introduce Mr. Scott Leinenweber, Vice President, Investor Relations, Licensing and Acquisitions.

Scott Leinenweber
SVP Licensing Acquisitions and Ventures., Abbott Laboratories

Good morning, and thank you for joining us. With me today are Robert Ford, Chairman and Chief Executive Officer, and Robert Funck , Executive Vice President, Finance, and Chief Financial Officer. Robert and Funck will provide opening remarks. Following their comments, we'll take your questions. Before we get started, some statements made today may be forward-looking for purposes of the Private Securities Litigation Reform Act of 1995, including the expected financial results for 2022. Abbott cautions that these forward-looking statements are subject to risks and uncertainties that may cause actual results to differ materially from those indicated in the forward-looking statements. Economic, competitive, governmental, technological, and other factors that may affect Abbott's operations are discussed in Item 1A, Risk Factors, to our annual report on Form 10-K for the year ended December 31, 2021.

Abbott undertakes no obligation to release publicly any revisions to forward-looking statements as a result of subsequent events or developments, except as required by law. On today's conference call, as in the past, non-GAAP financial measures will be used to help investors understand Abbott's ongoing business performance. These non-GAAP financial measures are reconciled with the comparable GAAP financial measures in our earnings news release and regulatory filings from today, which are available on our website at abbott.com. Note that Abbott has not provided the GAAP financial measure for organic sales growth on a forward-looking basis because the company is unable to predict future changes in foreign exchange rates which could impact reported sales growth. Unless otherwise noted, our commentary on sales growth refers to organic sales growth, which excludes the impact of foreign exchange. With that, I will now turn the call over to Robert.

Robert B. Ford
Chairman and CEO, Abbott Laboratories

Thanks, Scott. Good morning, everyone, and thank you for joining us. Today, we reported results of another strong quarter, including ongoing earnings per share of $1.15. Based on our performance through the first 9 months of the year, we increased our full year adjusted earnings per share guidance to $5.17-$5.23, which is more than 10% higher than the initial guidance we provided back in January. As you know, the macroeconomic conditions remain challenging. Inflation continues to be a stubborn force globally, though we've started to see some moderating impacts in certain areas of our businesses compared to earlier in the year. At the same time, the US dollar has continued to strengthen, including throughout the most recent quarter. COVID remains as unpredictable as ever, with intermittent surges continuing throughout the world.

Lastly, global supply chain dynamics, staffing shortages continue to impact our healthcare markets, though we're seeing steady signs of improvements. Over the last few months, we've made progress in several important areas following the temporary shutdown of our infant formula manufacturing plant in Sturgis, Michigan earlier this year. We restarted production at Sturgis in July with a focus on our EleCare and other specialty infant formulas. In September, we began production of several Similac products, which we expect will begin to reach retail store shelves over the coming weeks. We also boosted production in our global network to increase infant formula supply to the US. In fact, we delivered roughly the same volume of formula to our US customers this past quarter as we did during the three months prior to the recall.

Our number one supply priority was to the WIC, Women, Infant, and Children federal food assistance program to ensure that underserved participants would have access to infant formula. During the quarter, we also made leadership changes, both at our Sturgis site and in our quality organization, and we concluded a month-long investigation into the accusations that were made by a former employee. The investigation, which included extensive document reviews and interviews, concluded that the allegations about quality were unfounded. During the quarter, the same former employee dropped a federal OSHA complaint. Lastly, we conducted an analysis of the U.S. infant formula market and concluded that this country would benefit from more manufacturing capacity and redundancy. As such, we're moving forward with plans for a half billion dollar investment in a new U.S. nutrition facility for specialty and metabolic infant formulas.

We're currently in the final stages of determining the site location and will work with regulators and other experts to ensure this facility is state-of-the-art and sets a new standard for infant formula production. We recognize there's more to do, but feel confident in the progress we're making, and I wanna thank all the Abbott employees that have been working around the clock on this matter. I'll now summarize our third quarter results for our remaining businesses in more detail before turning the call over to Funck. I'll start with established pharmaceuticals or EPD, where sales increased more than 12% in the quarter. Strong performance was led by double-digit growth across several countries, including India, China, Brazil, and Vietnam, along with broad-based strength across several therapeutic areas.

EPD has now achieved double-digit organic sales growth since the beginning of last year, fueled by a steady cadence of new product launches and strong commercial execution. EPD has also expanded its profitability profile over the same time period, which is quite unique given the current macroeconomic headwinds. Moving to diagnostics, where COVID test sales of $1.7 billion were significantly higher than expectations, but lower compared to last year, which resulted in a modest decline in sales growth overall. The decline in COVID test sales compared to last year was driven by lower demand for laboratory-based tests. Whereas demand for our rapid tests, which include BinaxNOW, Panbio, and ID NOW, continues to be strong, with sales this past quarter at a similar amount to the third quarter of last year. Rapid tests have proven to be very important and highly practical tools.

They provide a quick and affordable way to test COVID almost anywhere and at any time, whether you're experiencing symptoms or just want to know your status before attending events or gatherings. Excluding COVID testing revenues, sales of routine diagnostic tests grew 6% in the quarter overall and even faster internationally, fueled by the continued global rollout of our Alinity instrument for immunoassay, clinical chemistry, and molecular testing. Lastly, I'll wrap up with medical devices, where sales grew 6.5% in the quarter globally. In the U.S., sales growth of approximately 11.5% was led by strong double-digit growth in electrophysiology, structural heart, and diabetes care. During the quarter in the U.S., cardiovascular procedure volumes were somewhat soft in July before strengthening in August and September.

Internationally, in addition to similar procedure volume trends, sales were negatively impacted by intermittent COVID lockdowns in China, as well as supply constraints in certain areas, most notably in electrophysiology. In diabetes care, sales of FreeStyle Libre exceeded $1 billion in the quarter, and our user base expanded to approximately 4.5 million users globally. In the US, where sales grew more than 40%, we initiated the full launch of Libre 3, which automatically delivers up-to-the-minute glucose readings with unsurpassed accuracy in the world's smallest and thinnest wearable sensor. Internationally, organic sales growth was impacted by a couple of transitory items, including supply constraints on Libre 1 in certain emerging markets, which we expect to improve over the next couple of months.

Secondly, a strategic choice we made in Germany to rapidly transition our large existing user base to our latest generation Libre 3 system, which temporarily reduced our focus on new user additions during the quarter in that country. We already transitioned well over half of our users, with the vast majority of the remaining users expected to move to Libre 3 by year-end. This move strategically fortifies our leadership position in the second-largest continuous glucose monitoring market in the world and further enhances our already strong strategic position as we work to bring the benefits of Libre to more and more people, including those with type two diabetes that are not reliant on insulin to manage their disease. In summary, despite the challenging environment, we achieved another strong quarter that significantly surpassed expectations, which reflects the strength of our diversified business model and execution.

Based on our strong performance for the first nine months of the year, we're once again raising our EPS guidance for the year. I'll now turn over the call to Robert Funck. Funck?

Robert Funck
EVP and CFO, Abbott Laboratories

Thanks, Robert. As Scott mentioned earlier, please note that all references to sales growth rates, unless otherwise noted, are on an organic basis, which excludes the impact of foreign exchange. Turning to our results. Sales increased 1.3% on an organic basis in the quarter. COVID testing-related sales were $1.7 billion, which, while stronger than anticipated, reflect a year-over-year decline versus sales in the third quarter of last year. Additionally, organic sales growth was negatively impacted by a temporary shutdown of manufacturing at our nutrition plant in Sturgis, Michigan, earlier this year. Excluding COVID testing-related sales and the U.S. sales impacted by the temporary manufacturing shutdown, total Abbott sales increased 6% on an organic basis in the third quarter. Foreign exchange had an unfavorable year-over-year impact of 6% on third quarter sales.

During the quarter, we saw the US dollar continue to strengthen versus several currencies, which resulted in a slightly more unfavorable impact on sales compared to exchange rates at the time of our earnings call in July. Regarding other aspects of the P&L, the adjusted gross margin ratio was 55.9% of sales, which reflects the impacts of the nutrition manufacturing disruption and inflation we've experienced on certain manufacturing and distribution costs across our businesses. Adjusted R&D investment was 6.1% of sales, and adjusted SG&A investment was 25.9% of sales in the third quarter. Lastly, our third quarter adjusted tax rate was 18.1%, which reflects an adjustment to align our year-to-date tax rate with our revised full year effective tax rate forecast of 15.5%.

The revised full year forecast is modestly higher than the estimate we provided in July due to a shift in the mix of our business and geographic income. Turning to our 2022 outlook. For the full year, we now forecast ongoing EPS of $5.17-$5.23, which is comprised of our year-to-date results through September, plus ongoing EPS guidance of $0.86-$0.92 for the fourth quarter. We forecast total company organic sales growth, excluding the impact of COVID testing-related sales, to be in the mid-single digits percentage for the fourth quarter.

Excluding U.S. sales impacted by the temporary manufacturing disruption, we forecast fourth quarter organic sales growth to be in the mid- to high-single digits for the remainder of our combined businesses, which includes medical devices, established pharmaceuticals, diagnostics, excluding COVID testing-related sales, and areas of nutrition not impacted by the disruption. We forecast COVID testing-related sales of approximately $500 million, which does not assume a COVID testing surge in the fourth quarter. Lastly, based on current rates, we expect exchange to have an unfavorable impact of approximately 7% on our fourth quarter reported sales. With that, we'll now open the call for questions.

Operator

Thank you. If you have a question at this time, please press star one one on your touch tone telephone. For optimal sound quality, we kindly ask that you please use your handset instead of your speakerphone when asking your question. Again, that's star one one to ask a question. Our first question comes from Robert Marcus from JPMorgan. Your line is open.

Robert Marcus
Managing Director and Senior Analyst, JPMorgan Chase & Co.

Oh, great. Congrats on the quarter, and thanks for taking the questions. Robert, maybe we could start, you know, we're already towards the end of 2022, and I think people's attention are really shifting to next year. Just with so many moving pieces, both in revenues and down the P&L with currency and inflation and COVID testing assumptions and so on. I was hoping, you know, sometimes at this point in the year, you might give us some early thoughts on next year. Anything you can provide to help us narrow the range of outcomes would be great. Thanks.

Robert B. Ford
Chairman and CEO, Abbott Laboratories

Sure. I mean, with all those topics, we could spend the whole call on it, right? I'll provide a broad framework that I can give you here. Obviously, the macro conditions are gonna remain challenging, right, Robert? I don't think that anybody right now, as we're planning going into next year, is forecasting that, you know, this is just gonna ease up, right? Specifically, I would say probably inflation, I don't expect to get better. I'd say the currency headwinds are very much kind of in play here for next year, right? Those are probably two of the big kinda macro impacts for us.

I still see a lot of opportunity for growth, as I have been talking about our business and our portfolio. You know, there's a clear path in my mind here for top line growth of high single digits. You can get there with, you know, a variety of looking at across our businesses. The medical devices, we've got a lot of upcoming launches.

Products that we have launched, so Libre 3, Amulet, Aveir, CardioMEMS, Navitor, we expect to be launching next year here in the U.S. EnSite X, our mapping system, launching a new ablation catheter into the market globally next year also. I'm probably sure there's more that I could kind of rattle off here in terms of devices. I think the device portfolio looks very strong as we go into next year. I expect the same kind of, you know, growth rate that we're seeing in EPD. I expect to see continued share capture that we're seeing in core diagnostics. Obviously, strong recovery in U.S. infant nutrition.

Like I say, you see that high single digit growth and the clear path just based looking at how those businesses will perform and how they're performing and the launches that we got upcoming. You mentioned COVID, right? That's the other piece of the business. High single digit growth excluding COVID. You know, COVID's an interesting one, Robert, where you know, I think over the last couple of years, we've been talking about the sustainability of COVID and, you know, many, many of you writing that you know, COVID testing will probably go away. Here we are in the third quarter, in the summer months with a $1.5-$1.6 billion number here in the third quarter.

I think that as we look I wanna see how the next few months look like. You know, I think Funck made a comment in terms of our forecast for Q4. We haven't really planned for a big winter surge. It's more of an endemic forecast for Q4, and I think that's the kind of endemic forecast that we'll see going into 2023. Right now, it's looking like COVID test sales are stickier than most have assumed. Those are the components on the top line. You know, down the P&L, as I've said, we're gonna be taking a close look at our cost structure. We have been.

We've increased that over the last couple of years, made the investments. We've talked about those investments. I'm looking to be able to get a lot of leverage out of those investments that we've made historically. You know, and at the top line, the way I've kind of laid out comes through and the leverage falls through, you're gonna see that sales growth falling through at, I'd say, pretty healthy margins. robert Funck is gonna invest in the areas that we know we've got good growth and high growth. Those get the investment dollars.

I think in the past, a lot of you have written about, you know, the big three of Abbott, whether it was Libre, Alinity and MitraClip, and those are still a big contributors of drive, a drive of growth. We have a new class of products, I guess I would call them the Fab Five, looking at TriClip, Aveir, Navitor, CardioMEMS and LAA. You know, these products combined are at an annual run rate of about half a billion dollars, growing 50%. Those will also receive the kind of investments to be able to kind of drive their growth since I think they're again in the early innings of growth for us.

We'll look at managing the P&L and our investments and our structures and choosing the areas where we're gonna continue to invest. Other areas, we'll see some of the leverage from the investments that we've made in the past. You know, as we go into 2023, to say that, you know, everything is, you know, fundamentally nothing's changed, I'd say true. Our markets are still very attractive. We've got leading positions in these very large high growth markets. I like the pipeline, and we've got a lot of ongoing and an upcoming launch activity. That I would say hasn't really changed. We're gonna have to be mindful, obviously, of the cost structure, of some of the inflation pressures and FX challenges we have.

We have a strong balance sheet, and we've talked about that, and that provides us a lot of strategic and financial flexibility as we go into next year. That's probably my best characterization here in the condensed version of 2023.

Robert Marcus
Managing Director and Senior Analyst, JPMorgan Chase & Co.

That's really helpful. And maybe one for Robert Funck. You know, the fourth quarter implied EPS guide came in a little bit lower than the street. You know, we also saw a much bigger FX headwind. How should we be thinking about the impact to the bottom line in third quarter? What's implied in fourth quarter? If we start thinking about our models for next year, Robert gave us the top line considerations. You know, how do we think about FX at current rates heading into next year? Thanks a lot.

Robert Funck
EVP and CFO, Abbott Laboratories

Yeah, certainly. You know, as you know, we've seen the U.S. dollar significantly strengthen this year, including throughout the third quarter. The biggest moves have been really in developed market currencies, you know, the euro, the pound, the yen. This is something that most, if not all, multinationals are dealing with, and certainly not unique to us. I think Robert, maybe these headwinds are a little bit underappreciated in terms of the impact here. You know, we always are looking to mitigate as best we can, but there's certainly gonna be a limit here in terms of what can be done. You know, we try to match our cost hedging program and take price where appropriate.

Robert B. Ford
Chairman and CEO, Abbott Laboratories

This year, at current rates, our full year headwind is a little bit more than $0.15 in terms of earnings. You know, about $0.10 of that is happening just in the fourth quarter alone. While there, you know, there are certainly other moving parts, that fourth quarter impact should give you a pretty good feel for the magnitude of headwind that's flowing into next year, particularly in the first two to three quarters of the year. You know, we'll provide our earnings guidance in January as we always do, and we'll contemplate currency rates, you know, at that time.

Robert Marcus
Managing Director and Senior Analyst, JPMorgan Chase & Co.

Thanks a lot.

Operator

Thank you. One moment for our next question. Our next question comes from Lawrence Biegelsen from Wells Fargo. Your line is open.

Lawrence Biegelsen
Senior Medical Device Equity Research Analyst, Wells Fargo

Good morning. Thanks for taking the question. Two product-related questions from me. First, I wanted to start with Libre. A lot going on there, Robert. You know, obviously the exciting news this quarter was the Type 2 basal LCD from CMS. So I'd love to hear your thoughts on that opportunity. You know, our back of the envelope math suggests that could be a billion-dollar opportunity for Abbott in five years. Love to hear, you know, if you agree. Just lastly, you know, on the vitamin C timing of that resolution, and any color, any additional color you want to provide on Libre. You know, I did catch in your prepared remarks, you talked about non-insulin patients. That was interesting. I did have one follow-up.

Robert B. Ford
Chairman and CEO, Abbott Laboratories

Sure. That's the catchall Libre question. Let me take the CMS one. It is very exciting. If I think about your model, you're probably more aligned maybe to my team, but I think my team is cutting it short in terms of what we could actually do with this indication, and I'll tell you why in a second. It is pretty significant. I mean, you got 4 million basal patients in the U.S., about a third of them are covered by CMS. This is probably gonna be in terms of the timing of public comments and you know, amount of time it's gonna take for CMS to make the decision and then the implementation date, et cetera.

This is probably more of a second half 2023 item, I would say. But it's pretty significant. You know, it's gonna expand CGM coverage by about 1.5 million patients on CMS. And as you probably know, Larry, you know, once CMS makes that determination, then there's a natural flow that will then move into the private commercial market. I'm looking at the opportunity of ultimately 4 million patients that, you know, will have potential to get some sort of coverage and benefit from the technology. Listen, I think that it's not surprising from the perspective of this coming up because we've been leading in the generation of data and evidence to support this proposal.

I think if you do a lit search on all the studies that have been done on CGM and then segment them between, you know, pump studies and basal studies and Type 2 studies and Type 2 with non-insulin studies, you're gonna see that Libre is at the head of all of those Type 2 studies. I think this is part of the investments that we've been making clinically to be able to show the evidence and how this benefits a broader population. With the value proposition that Libre has, you know, it provides us I think I know what your model is saying.

I just think that we'll have a disproportionate share of that. This is a market where whether it's in the U.S. or in Europe, it predominantly drives around primary care, primary care call point, primary care scale, specifically in the U.S. DMEs. This is a segment where we do very well. If you do an audit of prescriptions by physician class, Libre has taken about 80% market share of the primary care Rx's. The team's been working on that. I think it's a great opportunity. I think this kind of fuels into, you know, this notion of, this is a much larger market than, you know, has historically been contemplated as part of CGM.

That's what our strategy from the moment we entered the market has been thinking about it, right? We're not looking at sprinting quarter to quarter. We're looking at this over the long term and making the investments to be able to sustain this kind of growth rate. We announced manufacturing capacity expansions also in the quarter for diabetes care, because we believe that this is a, you know, we believe this is a $10 billion franchise by 2028. We believe that we've got pathway, you know, between 15 and 20 million users on this product. So we're resourcing our manufacturing, our scale, our commercial infrastructure, our service, our clinical investments to be able to support what I believe is a significant growth opportunity, and we intend to lead that.

I think your other question was on vitamin C. Yeah, we have completed the clinical work on the vitamin C. I'll provide updates at the appropriate time. I do recognize that this is an important, I would call short-term, medium-term kind of growth driver for us. If you think about our franchise, it's gonna be about basal, Type 2, and pump integration. Think of that the next kind of 2 years-3 years of key core growth drivers. I'd say more longer term to get to those numbers, you know, I made an announcement beginning of this year regarding looking at this outside of diabetes on our Lingo franchise, and that will then sustain our growth going forward.

We feel good about the study results. I'll be updating once we have something to update there. We are working on pump integrations outside the United States, and we'll have a pump integration launch by end of this year, beginning of next year into Europe with one of our pump partners. I think they're gonna benefit a lot from our user base that we have in those countries.

Lawrence Biegelsen
Senior Medical Device Equity Research Analyst, Wells Fargo

Robert, that was super helpful. Just for my follow-up, I'd love to get your reaction to the PASCAL data at TCT and the launch in the U.S. You know, specifically your thoughts on the greater durability effect they showed in with PASCAL. I know we haven't seen that in the MitraClip registries. Just any update on the locking issue we heard about this quarter. Thanks so much.

Robert B. Ford
Chairman and CEO, Abbott Laboratories

Yeah. It wasn't unexpected. You know, every time at TCT, there's always an expectation of a landmark study or an approval. That wasn't unexpected. They got approval for DMR. That's one of the smaller indications, about a third of the market. We've competed with PASCAL internationally already for a couple years. I expect to see some trialing in the U.S., and the question is gonna be how much of it is gonna stick. Internationally, MitraClip has done very well. We've held on to a good portion of our share. I think in Europe, we're kind of at that 80-20 split.

I think I expect some of those dynamics to play out here in the U.S., and I think MitraClip is gonna do very well. Regarding the dataset, I mean, it was I think it was 117 or 120 patients, I think it was maybe versus 63 of MitraClip. I mean, we've done over 150,000 implants, Larry. We've got great data on our products. We do have over 1,000 patients in the registry. I think the dataset's pretty small right now. We're working on our side. We're doing our investments in our clinical trials, investments in product advancements in MitraClip.

I think right now, I think the biggest opportunity is market expansion. We're gonna be driving a lot of that with the FMR indication. I think I said this in the last call. I think that, you know, one of the biggest impacts we had, for me, as I looked at our portfolio was regarding COVID, was not being able to benefit the FMR indication and the NCD. I think that's the biggest opportunity we have is market expansion and working to get those referral networks beefed up and driving that demand for further expansion. I think the locking mechanism. I think we had, you know, we took a field action.

I think that's so far going okay. Haven't had any kind of issues. Supply is back to normal.

Lawrence Biegelsen
Senior Medical Device Equity Research Analyst, Wells Fargo

Thanks so much.

Operator

Thank you. Our next question will come from Joanne Wuensch from Citibank. Your line is now open.

Joanne Wuensch
Managing Director, Citigroup

Good morning, and thank you for taking the question. I'd like to jump off a little bit from the MitraClip conversation and try and peel apart the double-digit growth in structural heart this quarter, a little bit stronger than we were looking for. How much of that is MitraClip versus demand for Portico versus maybe something else? How do you think about developing that segment a little bit further?

Robert B. Ford
Chairman and CEO, Abbott Laboratories

Sure. Well, I mean, I think we've talked about how important the structural heart portfolio was for us, even when we go all the way back to the acquisition of St. Jude and really building this franchise, and we've been intentional about doing that. MitraClip had a good quarter. We had a growth of about 6%. That was impacted a little bit in the U.S., but we had double digit, almost double digit growth internationally. If you kind of then back into that, you could see that some of the other parts of the portfolio are now starting to kind of, you know, as they're gaining in scale, Joanne, they're starting to have a stronger impact on the portfolio.

Amulet and Navitor internationally. I know you mentioned Portico, but I'd say it's probably more Navitor in Europe that did very well for us, and it continues to do pretty well. You know, as I say, we acknowledge that, you know, we're behind two market leaders here, but we're making the investments, and it's done pretty well. In Europe, I'd say we've got about an 8%-9% market share in Europe. In the accounts that we actually have Navitor in, we're close to kind of mid-teens. That product is very competitive, and we're looking forward to bring that here to the U.S.

We filed it with the FDA, and we expect to bring this to the market here in the first half of next year. Scott, maybe you could talk about Amulet and what we're seeing there also.

Scott Leinenweber
SVP Licensing Acquisitions and Ventures., Abbott Laboratories

Yeah. I'd say, Joanne, as Robert mentioned, it is kind of the remaining basket of that structural heart business that's driving a lot of the growth there, Amulet being a component of that. Launch in the U.S. continues to go very well. Nice traction. In particular, I would say in the early adopter accounts, those that started late last year, our share in those accounts is around 40% now at this point. It just shows you kind of once you get in there and get experience and have an opportunity to drive some deeper penetration, that you can really achieve a strong share position, and we're doing that in those early adopter accounts.

As we've added accounts over the first portion of this year, we'll look to do the same thing with them as we go forward. Great opportunity to build, seeing nice growth there. Like I said, like Robert said, kind of a handful of the other items along with TriClip, Navitor, and Amulet here that are driving growth in addition to what you're seeing and know is the long-term opportunity for MitraClip.

Joanne Wuensch
Managing Director, Citigroup

As my follow-up question, in nutrition, one of the things we talk with investors about is how do you think about the recovery in that segment once your supply is back up? Do you see yourself just returning to growth of the market rate or taking a good percentage of the share back? Or any guidance you could give us we model forward would be helpful. Thank you.

Robert B. Ford
Chairman and CEO, Abbott Laboratories

Sure. I would say, we've had a situation like this back in 2010, and we've seen other competitors have situations like this, Joanne. In terms of the share recovery process, I'd say there's a couple key things in terms of consideration. When you think about doing those modeling, it's looking at your share of the WIC program, you know, your ability to continue to call on pediatricians and your share in the hospitals. I would say we've disproportionately focused in this quarter with our global supply network to focus on those channels.

You know, one of the challenges with that is you know, the WIC channel is a lower price channel than what I would call the non-WIC channel. That's probably where we made a decision to take the volume that we had, and like I said in my opening comments, we actually supplied to the market this quarter what we supplied in the three months prior to the recall. It's just the mix of that supply was overly gated towards the WIC states and the WIC contracts that we had. We made a commitment to those states that they would not have backward supply shortages. We focused on that.

I think by focusing on that, we not only you know lived up to our commitments and the contracts that we put in place, but that's gonna obviously be a base for us as we go into this quarter and into next quarter. If you look at the Nielsen data, you do see share recovery. I'd say we probably lost about 20 share points from the recall. I think the last read that I saw in September was we got half of it back. That is a mix.

This will go to the mix piece where on the WIC side, we've recovered all of our share, and now we're gonna take our capacity and start moving it into the non-WIC channel with a non-WIC configuration. Like I said, you know, we've intentionally made these decisions in terms of how we're supplying the market. I think by doing that, just naturally, with the work that our teams are doing, we'll start to see the share recovery build, you know, month-over-month. That's probably how to think about it.

Joanne Wuensch
Managing Director, Citigroup

Thank you very much.

Operator

Thank you. One moment for our next question. Our next question comes from Joshua Jennings from TD Cowen. Your line is open.

Joshua Jennings
Managing Director and Senior Analyst, TD Cowen

Hi, good morning. Thanks for taking the questions. Robert, I wanted to ask about the COVID testing franchise and just the strength in 2022 and thinking about the comp for 2023. Is there anything you can share in terms of contracts that are in place for 2023 and what that base could look like, whether contracts in 2022 could roll over into 2023? I know it's impossible to forecast utilization or uptake of COVID testing next year, but if there's any base commentary you can provide, that would be helpful. Just have one follow-up.

Robert B. Ford
Chairman and CEO, Abbott Laboratories

Looking at the market between government contracts and non-government contract is something that we spent a lot of time this year doing because obviously those government contracts, you know, they're high volume, and you know, they ultimately skew a little bit of kind of the run rate as we're trying to kind of run rate this. If you look at our Q4 number that we're forecasting is really what I would call an endemic state, right? About a half a billion dollars across the world, across all of our platforms, in a winter season without necessarily forecasting the kind of surge that we saw last year. In that number, we do not have any significant government contracts.

Now, what governments have realized is that, you know, they do need to make some investments, and they do need to hold some level of testing inventory, you know, in their countries. We have active conversations with a lot of governments, and they recognize and realize in Abbott's ability to scale up, you know, and scale up pretty fast. We've got plenty of capacity, and they know that. They know the value of our product. They work very well in terms of determining COVID and, you know, the new variants, et cetera. We don't have any significant number in Q4 of this year. We think that that's the kind of right kind of run rate from an endemic standpoint.

You know, if there is a surge, if governments realize that they do need to procure more testing, we've got the product, we've got the reliability of the product, and we've got the reliability of the supply, and they know that. We're in a good position there.

Joshua Jennings
Managing Director and Senior Analyst, TD Cowen

Excellent. Just one follow-up on Libre. You mentioned just the path to achieving full iCGM status, and understand there's a segment of the CGM market that will open up for Libre. Was wondering if you could just share your thoughts on the potential impact to clinician sentiment towards accuracy of the platform, payer sentiment in terms of whether there could be any, you know, formulary prioritization decisions, considering the pricing. Then on the other side of that, how are you any new thoughts on pricing for Libre three, particularly in this inflationary environment? Thanks for taking all the questions.

Robert B. Ford
Chairman and CEO, Abbott Laboratories

Sure. Well, listen, this is an important segment, right? You know, obviously the vast majority of CGM users and the vast majority of future potential users are people that are either injecting insulin with pens or syringes, or not even using insulin, right? We recognize that this is an important segment. We're doing—like I said, we completed the work on Libre 2 regarding the vitamin C. We'll be updating the market and our partners, you know, as we go through that process with the agency. We also believe that there's potential to innovate even further in that pump integration, right? We talked about this last call.

We announced this at the ADA in June, which is the creation of a dual analyte sensor, a glucose ketone sensor. You know, everybody, all the key opinion leaders that I've spoken to, I guess you're referring to believe that, you know, this would be the go-to sensor for pump integration because the ketone functionality provides the added safety feature that would be required, right? If there's some sort of interruption in insulin delivery from the pump, what is understood clinically is that the ketone levels will rise earlier than the glucose levels. To be able to have that ketone level, that continuous ketone level measurement, is an added safety feature for that pump environment.

I think it does provide, I guess, a step ahead in terms of innovation in terms of pump integration. Regarding the accuracy, I mean, I think it's commonly understood and the data is very clear in terms of FreeStyle Libre 3. I mean, even FreeStyle Libre 2, but FreeStyle Libre 3 being a definitive, you know, best in class accurate sensor. It's the only CGM sub-8 MARD. So, I don't think we have that, you know, that issue. So, it's an important segment, and we're gonna be investing in it, and we're gonna, you know, our goal is to actually provide something that's even more advanced and more beneficial. So...

Oh, it was pricing. Yeah, Libre 3 pricing, Libre 2 pricing, Libre 1 pricing, you know, it's practically all the same, Joshua. The more volume we can get onto Libre 3, the more we can kind of lower those COGS. We have a parity pricing right now.

We think that pricing strategy, you know, as I said last year, as the international markets or even in the US, you know, people have challenges either with co-pays in the US or with, you know, formularies and reimbursement decisions internationally. I think that our value proposition is very strong, and it's gonna prove itself out very clearly, you know, as single payer systems start to look at how to fine-tune their budgets and get more done, either with less or with the same amount. I think that our value proposition, consumer-friendly product with best in class accuracy, feature set, that, you know, no real gaps, and our pricing strategy, I think it's a complete value prop.

Joshua Jennings
Managing Director and Senior Analyst, TD Cowen

Appreciate it. Thanks, Robert.

Operator

Thank you. One moment for our next question. Our next question comes from Vijay Kumar from Evercore ISI. Your line is open.

Vijay Kumar
Senior Managing Director, Evercore ISI

Hey, guys. Thanks for taking my question. Robert, maybe my first one for you. The headline organic ex COVID in 3Q was, you know, 3%-ish, low singles. You know, when you back out some of these, you know, the supply chain impacts, I think you mentioned Germany, nutrition, what was the underlying organic growth? And when can we get back to an environment where there is no mismatch in this headline organic and underlying rate? It's a clean number. Maybe just talk about that cadence to normality.

Robert B. Ford
Chairman and CEO, Abbott Laboratories

It was high single, mid to high single, once you do all those exclusions. I don't like doing that. I mean, I get that it's important to be able to isolate what the challenges are and what the issues are and, you know, are they more transitory, or are they more kind of sustained issues in the business. I would say, you know, the issues that we've had, the challenges we've had in this quarter regarding supply chain, they're fairly, I'd say from a med device perspective, they're pretty significant, and they kind of had the impact that we saw in our med device business.

I think if you had looked at the kind of back orders that we had, whether it was Libre 1 and some of the back orders we had in EP, we would be high single digits. If you back out, you know, these issues, you know, mid to high overall for the company. You know, your question of when do we get into kind of normal organic? You know, I think part of the challenge here is COVID's at play. You know, as that base becomes smaller than what it is this year, I mean, this year, we'll probably do very much close to the same amount of COVID test sales that we did kind of last year.

As we move into next year, and that becomes smaller than this year, we'll see a little bit of an impact on, you know, on that overall growth rate. As I said, I think in Robert's question, I see high single digit growths once you back out of COVID. COVID will be just the determining factor there. Base non-COVID high single digits next year.

Vijay Kumar
Senior Managing Director, Evercore ISI

That's helpful. Maybe one on the financial side. I think, you know, gross margins were down Q-on-Q. I'm wondering what was the FX incremental inflationary impact? You know, I think Robert Funck mentioned $0.10 of FX impact in Q4. Should we annualize that to about, you know, $0.40 of FX impact for next year? I'm not sure how to think about FX and inflation, inflationary impact for next year. We didn't talk about Lingo. You know, shouldn't that be an incremental driver here in 2023? Thank you.

Robert Funck
EVP and CFO, Abbott Laboratories

Well, let me, Vijay, I'll take the exchange first. I mean, you know, I wouldn't necessarily take that $0.10 impact in the fourth quarter and extrapolate that for the full year of next year, but certainly through the first three quarters, you would expect to see that. But then in the fourth quarter, you're gonna kind of be at those rates that we currently are at. But again, it is, you know, it is gonna be a significant headwind for us next year. On inflation, you know, definitely, we're seeing the impacts there. Like others, the biggest impacts we've seen are really around commodities, other manufacturing input costs and logistics.

We've incorporated about another $100 million impact on gross margin in our current guidance. That's about $1 billion for the year. Call it maybe 240, probably a little more than 240 basis points on the gross margin. As Robert said, we, you know, we've seen a little bit of moderation in the rate of increase in the third quarter compared to where we were earlier in the year, and we're trying to take some price to offset that, really more in our consumer-facing businesses.

You know, kind of given the way that inflation has hit us over the course of this year, the inventory that we purchase and manufacture this year at these higher costs, you know, will definitely negatively impact us next year when that inventory gets sold, even if inflationary pressures start to come down kind of, as we get into next year.

Robert B. Ford
Chairman and CEO, Abbott Laboratories

On your question on Lingo, Vijay, you know, we have factored in a launch into next year. We have not factored that launch here in the U.S., so it is an international launch. It's a different business model as I've talked about it, more of a direct-to-consumer, wellness, subscription model.

We're on target here to come out of the gates of that in Q1. We are gonna be launching into a what I would call a little bit of a challenging environment, so we've taken that into consideration here. I think that the long-term growth opportunity of building this kind of business, a wellness subscription-like model, with you know with the platform that we built and the scale that we have, I think is a great growth opportunity for us. We do have it factored into next year, probably, launching in the beginning of the year and then building from there.

We'll be launching, you know, in a, like I said, in a challenging environment, but I still think it's the right thing to do from a long-term perspective.

Vijay Kumar
Senior Managing Director, Evercore ISI

Thank you, guys.

Robert B. Ford
Chairman and CEO, Abbott Laboratories

Operator, we'll take one more question.

Operator

Thank you. We'll take our last question from Travis Steed from Bank of America. Your line is open.

Travis Steed
Managing Director and Senior Equity Analyst, Bank of America

Hey, thanks for taking the question. I did want to ask on China, how you see the recovery shaping up there? That's gonna be another headwind next year, and any new VBP that you see coming up in China?

Robert B. Ford
Chairman and CEO, Abbott Laboratories

Yeah. It is gonna be a little bit of a headwind. You can think about it as either currency and VBP. We've gone through this in some other parts of our business, so we do expect, you know, this value-based procurement or pricing here to play out. I think the next area that, you know, that we're looking at. We've gone through it with stents last year or a year and a half ago. The next area that we're looking at is probably on the electrophysiology side. That's probably the next category that's up. You know, it's interesting, as we've been looking at this, there's, you know, there's definitely interesting impacts in terms of ranges of these pricing.

We actually have gone through some of it in pharmaceuticals also. It'll range from 30%-80% in terms of pricing. Really the magnitude here depends on whether, you know, it's a national or regional process. You know, some of the categories have been more regional, and they tend to be a little bit lower. It also depends on the number of participants that exist in that category. As I look at the EP side, we've also seen that when there are more system...

Like a system-based approach, Travis, so think capital, think about the technical support and the infrastructure associated support that those tend to be a little bit on the lower end of that range versus to be on the higher end of that range. That's probably what we've got contemplated for VBP next year is more on the EP side.

Travis Steed
Managing Director and Senior Equity Analyst, Bank of America

No, that's helpful. I did wanna ask about the M&A environment too, since it hasn't come up yet on this call. Also kinda how it relates to your thinking the device growth longer term, if you're still able to grow at the higher end of med tech, and if the Fab Five, as you call it, is enough to do that, or if you need to augment device growth with M&A, you know, over time.

Robert B. Ford
Chairman and CEO, Abbott Laboratories

No, I don't feel that I need to do M&A to be able to sustain that high single digit growth that we've been posting pretty consistently on devices. I did say in the last call that, you know, we're interested and we're being prudent about that interest. The interest has increased. You know, we actively assess all the opportunities here. As I've said, just because we have a strong balance sheet and we've got a lot of flexibility, we're still gonna make sure that we're going about this from a strategic perspective, and we're going about it from a financial perspective. Obviously valuations come down somewhat, and that helps on the financial modeling and attractiveness side from it.

I would say they probably need to stabilize a little bit, these valuations, so that you can engage what I would call just meaningful discussions here. I think as those stabilize, I think you'll see the environment pick up here in terms of M&A. We're in a good position. Don't need to do M&A, but there's a lot of opportunities out there for us, and we're gonna apply you know that consistent framework of you know strategic and financially disciplined in terms of how we look at them. Okay?

Travis Steed
Managing Director and Senior Equity Analyst, Bank of America

F. Yeah, thank you.

Robert B. Ford
Chairman and CEO, Abbott Laboratories

I'll just sum up here. Q3 was probably our very challenging quarter for us, probably our most challenging. Obviously the impact of inflation and supply chain and some of the back orders that we encountered was a headwind. Some of the FX as we go forward also will be a headwind. You saw the portfolio strength and the execution here coming through all those challenges and delivering not only in the quarter but also for the full year as evidence of our full year raise here also. It's also provided us an opportunity to make some strategic choices to strengthen our business and to strengthen our position and build our momentum.

I guess, you know, to Robert's comment in the beginning about how everybody's shifting to 2023, so are we. You know, we made some choices and some decisions here to be able to, you know, prepare us and build our momentum and strengthen our position as we go into 2023. I saw a nice recovery in the institutional businesses and our pipeline here that we talked a little bit about is gonna sustain that growth acceleration. There's a lot of organic growth opportunities that we've got in 2023, and I highlighted here how I see a clear path for high single digit revenue growth.

On top of that, we've got a strong balance sheet, and that's gonna allow for a very balanced capital deployment to our shareholders and also allow us to fuel future growth. With that, I'm gonna wrap that up. Thanks.

Scott Leinenweber
SVP Licensing Acquisitions and Ventures., Abbott Laboratories

Thank you, operator, and thank you for all of your questions. This now concludes Abbott's conference call. A webcast replay of this call will be available after 11 A.M. Central Time today on Abbott's investor relations website at abbottinvestor.com. Thank you for joining us today.

Operator

Thank you. This concludes today's conference call. Thank you for your participation. You may now disconnect. Everyone, have a wonderful day.

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