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Perrigo


Perrigo Company plc is an Irish-domiciled multinational corporation that develops, manufactures, and markets over-the-counter (OTC) consumer self-care products, including private-label pharmaceuticals, nutritional products, and infant formulas.
Founded in 1887 in Allegan, Michigan, by brothers Luther and Charles Perrigo as a general store, the company expanded into manufacturing in the early 20th century and became a pioneer in store-brand OTC medications, growing to serve as the largest U.S. provider of such products and a top-10 player in the European consumer self-care market.
Perrigo's business model emphasizes affordable, high-quality alternatives to branded products, with operations spanning North America, Europe, and other regions, supported by a portfolio of facilities focused on self-managed health solutions.
The company has encountered regulatory challenges, including U.S. Food and Drug Administration warnings for manufacturing lapses at its Michigan facility leading to drug mix-ups, as well as antitrust litigation alleging anticompetitive agreements in the infant formula sector.

History

Founding and Early Development (1887–1980s)

L. Perrigo Company was founded in 1887 in Allegan, Michigan, by brothers Luther and Charles Perrigo, who had relocated from New York a few years earlier. Luther, operating a general store and apple-drying business, began packaging generic home remedies—such as epsom salts, sweet oil, and bay rum—along with patented medicines, for distribution to other rural general stores to build customer loyalty through private labeling. This initial model focused on repackaging affordable household health products rather than branded manufacturing. The company was formally incorporated in 1892 as L. Perrigo Company, with Luther Perrigo serving as its first president; it remained family-owned for the next 90 years, with five of the first seven presidents being Perrigo descendants. In the 1920s, Perrigo expanded into private-label imprinting, customizing labels with individual store names on products like aspirin. By 1921, it established its first manufacturing facility in Allegan, enabling in-house production beyond mere repackaging. During the , Perrigo shifted its customer base from general stores to larger regional and drug chains, including early clients like the K & W group and Sam's, and secured its first major private-label contract in the mid-decade, solidifying its role in affordable healthcare supply. Post-World War II, under leadership including Ray Perrigo and William L. Tripp Sr. in the 1950s, the company transitioned from repackaging to full-scale manufacturing of quality s and beauty aids, emphasizing store-brand over-the-counter products. In the 1960s and 1970s, Perrigo broadened its market to include grocery chains and mass merchandisers; William L. Tripp Jr. led significant growth from 1967 onward, quadrupling income and employee numbers by 1969 under his father's earlier influence. By 1978, under president Robert J. Swaney, sales tripled through acquisitions of smaller firms and expanded distribution, positioning Perrigo as the nation's largest private-label manufacturer of health and beauty products by 1980. The Perrigo family divested ownership to company management in the early 1980s after nearly a century of control, with Michael Jandernoa assuming the presidency in 1984 amid ongoing focus on over-the-counter generics.

Expansion Through Acquisitions (1990s–2010s)

In the 1990s, Perrigo shifted focus toward vertical integration and diversification by acquiring manufacturers of store-brand personal care and pharmaceutical products, aiming to bolster domestic production capacity and eliminate key competitors. In January 1992, the company purchased Cumberland-Swan, Inc., a Tennessee-based producer of store-brand personal care items and vitamins, for $35 million, which expanded its contract manufacturing services. This was followed in December 1994 by the $33 million acquisition of Vi-Jon Laboratories, Inc., a leading U.S. maker of private-label personal care products, further strengthening Perrigo's position in that segment. International expansion accelerated in the late , with Perrigo targeting emerging markets for OTC pharmaceuticals. In late 1997, it acquired an 88% stake in Química y Farmacia, S.A. de C.V. (Quífa), a manufacturer of over-the-counter (OTC) and prescription drugs, for $17 million, gaining non-U.S. manufacturing facilities and entry into Latin American channels. By 2001, Perrigo entered the European market through the $44 million purchase of Wrafton Laboratories Ltd. in the , a supplier of store-brand pharmaceuticals to grocery and drug retailers, which established production capabilities for UK private-label needs. The 2000s saw continued acquisitions to deepen category expertise and geographic reach, particularly in OTC and nutritional products. In 2005, Perrigo acquired Agis Industries Ltd., an Israeli firm involved in active pharmaceutical ingredient (API) development, pharmaceutical manufacturing, and medical diagnostics, enhancing its technical capabilities in specialty areas. In 2008, the company bought Galpharm Healthcare, Ltd., a UK-based producer of OTC store-brand items, which reinforced its supermarket and pharmacy distribution in Europe. A pivotal deal in the early 2010s was the March 2010 acquisition of PBM Holdings, Inc., for $808 million in cash, making Perrigo the dominant player in store-brand infant formula and baby foods across the United States, Canada, Mexico, and China, with added manufacturing assets in Vermont and Georgia. These moves from the 1990s through the 2010s diversified Perrigo's portfolio beyond basic generics into higher-margin categories like infant nutrition and international OTC, while building a global supply network that supported store-brand growth amid rising retailer demand.

Tax Inversion, Restructuring, and Divestitures (2010s–2020s)

In July 2013, Perrigo announced its acquisition of Elan Corporation plc, an Irish biotechnology firm, for approximately $8.6 billion in a cash-and-stock deal, which was structured as a tax inversion to relocate the company's tax domicile from the United States to Ireland. The transaction, completed on December 18, 2013, reduced Perrigo's effective corporate tax rate on certain profits from the U.S. statutory rate of 35% to Ireland's 12.5%, while establishing a new holding company in Dublin. This move was part of a broader strategy among U.S.-based multinationals to access trapped foreign earnings and optimize global tax liabilities amid high domestic rates. The inversion faced subsequent challenges, including a 2018 assessment by tax authorities demanding €1.6 billion ($1.8 billion) in back es related to the integration and profit allocations, which Perrigo contested as undermining the deal's intended benefits. In 2015, N.V. launched a hostile $26 billion bid for Perrigo, aiming to its domicile for further tax efficiencies, but Perrigo's board rejected the offer, citing undervaluation and strategic misalignment. These events highlighted risks of inversion strategies, including regulatory scrutiny and , though Perrigo retained its headquarters. Amid post-inversion integration pressures and shifting market dynamics, Perrigo pursued restructurings in the late 2010s, including sales force realignments, brand portfolio prioritization, and manufacturing insourcing to cut costs and enhance efficiency. By the 2020s, the company accelerated divestitures of non-core assets to refocus on consumer self-care products: in June 2020, it sold its UK-based Rosemont Pharmaceuticals generic prescription business for £120 million ($156 million); in July 2024, it divested the HRA Pharma Rare Diseases unit to Esteve for up to €335 million in total consideration; and in July 2025, it agreed to sell its European dermacosmetics business to a KKR-managed entity for up to €327 million. These actions supported Perrigo's "Optimize and Accelerate" strategic plan launched in February 2023, which emphasized portfolio streamlining, operational agility, and growth in over-the-counter segments, alongside a July 2025 organizational update involving category realignments and cost optimizations to counter competitive pressures. The divestitures generated capital for reinvestment, though they incurred restructuring charges, reflecting a shift from diversified pharmaceuticals toward higher-margin, consumer-oriented operations.

Business Operations

Current Segments

Perrigo Company plc operates primarily through two business segments: Consumer (CSCA) and Consumer (CSCI). These segments focus on the development, manufacturing, marketing, and distribution of over-the-counter (OTC) consumer products, emphasizing private-label offerings for retailers. In 2024, the company's total net from continuing operations reached $4.37 billion, with CSCA generating the majority of through in the U.S. and other markets. The Consumer Self-Care Americas (CSCA) segment encompasses Perrigo's core operations in North and Latin America, where it produces a wide range of private-label OTC products including cough and cold remedies, analgesics, digestive health aids, oral care items, and vitamins and supplements. This segment leverages 11 U.S.-based manufacturing facilities, which account for approximately 85% of Perrigo's domestic OTC production volume, positioning the company as the largest U.S. manufacturer of such products by volume. Key categories driving CSCA performance include upper respiratory, nutrition, and healthy lifestyle products, though challenges such as declines in digestive health sales have impacted growth. The Consumer Self-Care International (CSCI) segment handles operations outside the Americas, primarily in Europe and other international markets, distributing similar private-label self-care products tailored to regional needs, such as skincare, hair care, and infant nutrition. This segment benefits from Perrigo's global supply chain but faces currency fluctuations and varying regulatory environments. In recent quarters, CSCI has shown resilience amid divestitures of non-core assets, contributing to overall portfolio optimization. Following strategic divestitures, including the sale of its prescription pharmaceuticals business, Perrigo has streamlined its focus exclusively on these self-care segments to enhance operational efficiency and profitability. This , completed in the early 2020s, has allowed greater emphasis on high-margin OTC categories amid rising consumer demand for affordable, store-brand alternatives.

Products and Market Focus

Perrigo specializes in the development, manufacturing, and distribution of consumer products, emphasizing over-the-counter (OTC) solutions for health and wellness. The company's portfolio centers on affordable, high-quality and branded items that address common self-managed conditions, including and cold remedies, analgesics, gastrointestinal aids, and nutritional supplements. This focus stems from a strategic shift toward core categories, following divestitures of non-core assets to enhance margins and growth potential. Perrigo operates through two primary reporting segments: Consumer Self-Care Americas (CSCA) and Consumer Self-Care International (CSCI). The CSCA segment, covering the United States, Mexico, and Canada, primarily produces private label products for retailers, including cough, cold, and allergy treatments; analgesics; gastrointestinal products; smoking cessation aids; infant formula; and select food items. In contrast, the CSCI segment targets international markets, particularly Europe, with branded offerings such as natural health products, vitamins, personal care items, derma-therapeutics, and lifestyle solutions alongside similar OTC categories like cough and cold remedies and smoking cessation products. These segments collectively generate thousands of stock-keeping units (SKUs) in liquid, solid, and semi-solid forms, supported by extensive research and development to meet regional consumer needs. The company's market emphasis lies in providing accessible self-care alternatives to branded pharmaceuticals, prioritizing cost-effectiveness without compromising efficacy or safety. In the Americas, private label dominance allows Perrigo to capture significant share in retailer channels, while in Europe and beyond—including Asia and Australia—branded products build consumer loyalty through established trademarks. Recent performance highlights growth in key areas like nutrition, upper respiratory treatments, and healthy lifestyle products, offsetting declines in digestive health, as reported in second-quarter 2025 results. Perrigo's supply chain expertise enables scalable production, with facilities inspected to regulatory standards, ensuring broad availability at pharmacies, retailers, and e-commerce platforms.

Global Operations and Supply Chain

Perrigo operates a network of manufacturing facilities concentrated in North America and Europe, supporting its production of over-the-counter (OTC) medications, infant formulas, and nutritional products. In the United States, the company's primary hub is in Allegan, Michigan, where it established its first manufacturing plant in 1921 and maintains multiple sites, including Plant 6 at 502 Eastern Avenue, focused on consumer healthcare goods. Additional U.S. facilities include sites in Vermont, Ohio, and Wisconsin for nutrition manufacturing, enabling efficient domestic supply for store-brand products. Historically, Perrigo operated a nutritional supplement facility in Greenville, South Carolina, which achieved NSF registration for quality standards in 2002. In Europe, Perrigo's footprint includes several sites in the United Kingdom and Ireland, such as Barnsley in South Yorkshire, Braunton in North Devon, Leeds in West Yorkshire, Pimlico in London, and Dublin, positioning it as a top-10 player in the European consumer self-care market. The company also maintains regional operations in Belgium (in Dutch and French) and Australia, facilitating distribution across international markets. This geographic spread supports Perrigo's role as the largest U.S. provider of store-brand OTC and infant formula products while extending reach into global self-care segments. Perrigo's supply chain strategy emphasizes optimization and resilience, integrated into its 2023-launched "Optimize and Accelerate" three-year plan, which targets 3% annual organic net sales growth, 5% adjusted operating income growth, and enhanced efficiency through supply chain reinvention. Leadership transitioned in June 2025 with the appointment of Matt Winterman as Executive Vice President of Global Operations and Supply Chain, succeeding Ron Janish after his retirement on September 30, 2025; Winterman, formerly SVP of Global Supply Chain at AstraZeneca, brings over 20 years of experience managing complex portfolios including 5,000 SKUs. The strategy addresses challenges like logistics disruptions and inflation, with a focus on network redesign led by roles such as Senior Director of Supply Chain Network Strategy in Dublin. Sustainability forms a core element of Perrigo's supply chain management, with commitments to net-zero greenhouse gas emissions across operations and the full supply chain by 2040, including Scope 1, 2, and 3 reductions. Membership in the Pharmaceutical Supply Chain Initiative (PSCI) provides tools for global risk mitigation, ethical sourcing, and environmental protection, amid efforts to quantify supply chain climate impacts through retailer partnerships. These initiatives aim to ensure fair labor, reduce environmental footprints, and build resilience against disruptions like those experienced in U.S. logistics post-2020.

Leadership and Governance

Executive Team

Perrigo Company plc's executive management team, as outlined on the company's official website, is responsible for overseeing strategic direction, operations, and key functional areas in the consumer self-care products sector. The team is led by Patrick Lockwood-Taylor, who has served as President and Chief Executive Officer since June 30, 2023. Key members include:
NamePositionKey Details
Charles AtkinsonExecutive Vice President, General Counsel and SecretaryOversees legal affairs and corporate governance.
David BallExecutive Vice President, Chief Brand and Digital OfficerManages branding, marketing, and digital initiatives.
Eduardo BezerraExecutive Vice President and Chief Financial OfficerHandles financial planning, reporting, and investor relations.
Roberto KhouryExecutive Vice President and Chief Commercial OfficerDirects global commercial strategy and sales.
Abbie LennoxExecutive Vice President and Chief Scientific OfficerAppointed in January 2025; focuses on scientific research and product development.
Rob WillisExecutive Vice President and Chief Human Resources OfficerLeads HR strategy, talent management, and employee relations.
Matt WintermanExecutive Vice President, Product Supply, Operations Strategy and Transformation OfficerAppointed in June 2025 to succeed Ronald Janish upon his retirement on September 30, 2025; brings over 20 years of supply chain experience.
This structure supports Perrigo's focus on over-the-counter health and hygiene products amid ongoing operational transformations.

Key Strategic Decisions

In 2018, Perrigo appointed Murray S. Kessler as president and CEO to execute a consumer-focused strategy, emphasizing innovation, mergers and acquisitions, and continuous portfolio optimization to transition from a primarily pharmaceutical-oriented model to one centered on over-the-counter self-care products. This shift involved 14 M&A transactions and divestitures to reconfigure the product portfolio, alongside resolving a $4 billion tax and legal liability overhang accumulated from prior operations. Kessler's leadership culminated in the February 2023 launch of the three-year "Optimize and Accelerate" strategic plan, which targeted 3% net sales growth, 5% adjusted operating income growth, and 7% adjusted diluted EPS growth through 2025, supported by portfolio reconfiguration including 12 transactions over the prior four years and the acquisition of Héra SAS to bolster European consumer healthcare presence. The plan prioritized scaling molecule production efficiently across markets while maintaining core pillars of quality, customer service, innovation, and cost discipline. Following Kessler's retirement on July 31, 2023, subsequent leadership under interim and permanent successors continued portfolio streamlining, including the divestiture of the dermocosmetics business in 2024 as part of the "Three-S" initiative (Stabilize, Streamline, Strengthen) to concentrate resources on high-margin OTC segments. In July 2025, the company announced an organizational update restructuring into three units—Consumer Self-Care International (CSCI), Consumer Self-Care Americas (CSCA), and Rx—to enhance agility, align operations with self-care scaling goals, and drive sustainable growth without altering 2025 financial guidance. This included leadership transitions in global operations and supply chain to integrate expertise in efficiency and strategy.

Financial Performance

Historical Overview

Perrigo Company, originally established in 1887 as a packer of botanical drugs, experienced modest financial growth in its early decades, focusing on private-label pharmaceuticals and household products. By the late 1980s, following its initial public offering in 1984 and subsequent expansion into store-brand manufacturing, annual revenue reached $146 million in fiscal 1988. This period marked the beginning of accelerated growth driven by demand for generic and over-the-counter (OTC) alternatives to national brands, with sales tripling under key leadership changes in the late 1970s and early 1980s. The 1990s saw robust revenue expansion through strategic acquisitions and market penetration in private-label OTC products. Sales surged from $146 million in 1991 to $669 million by 1994, bolstered by purchases such as Cumberland-Swan, Inc. for $35 million in 1992 and Vi-Jon Laboratories, Inc. for $33 million in 1994, which enhanced manufacturing capabilities and product diversification. However, growth slowed in 1995–1996 amid intensified competition and weaker seasonal demand for cold and flu remedies, leading to declining profits. By fiscal 2003, revenue had recovered to $826 million, supported by further international expansions like the 1997 acquisition of an 88% stake in Química y Farmacia, S.A. de C.V. for $17 million and ongoing focus on generics. Challenges persisted, including a $51.6 million net loss in 1998 from personal care segment restructuring and $21 million in costs from a 2000 phenylpropanolamine product recall. Entering the 2010s, Perrigo's financial trajectory shifted toward aggressive acquisitions to build scale in generics and international OTC markets, propelling revenue from approximately $2.7 billion in 2010 to a peak of $5.281 billion in 2016, fueled by deals such as Paddock Laboratories and the $8.7 billion acquisition of Omega Pharma in 2015. This era included the 2013 tax inversion to Ireland, which aimed to optimize costs but later drew regulatory scrutiny. Revenue subsequently moderated amid integration challenges, patent cliffs, and divestitures, falling to $3.870 billion in 2019 before stabilizing around $4 billion annually—$4.088 billion in 2020, $4.139 billion in 2021, $4.452 billion in 2022, $4.656 billion in 2023, and $4.373 billion in 2024. Net income has shown volatility, with frequent losses in recent years attributed to goodwill impairments, supply chain disruptions, and infant formula recalls, such as the 2022–2023 events impacting profitability. Overall, Perrigo's financial history reflects acquisition-driven expansion tempered by operational and regulatory headwinds, with a compound annual revenue growth rate averaging mid-single digits from the 1990s through the 2010s before flattening. In the early 2020s, Perrigo experienced revenue growth amid heightened demand for over-the-counter health products during the COVID-19 pandemic, with annual net sales rising from $4.1 billion in 2021 to a peak of $4.7 billion in 2023. This expansion reflected organic increases in consumer self-care segments, though tempered by broader economic pressures including inflation and supply chain disruptions. By fiscal year 2024, however, net sales declined 6% to $4.4 billion, primarily due to strategic divestitures, exited product lines, and actions to bolster the infant formula business following earlier recalls and market shifts. Profitability faced headwinds, with reported operating income dropping 26% to $113 million in fiscal 2024 from $152 million the prior year, driven by higher costs and one-time restructuring expenses. Net income turned negative at -$172 million for 2024, reflecting ongoing investments in supply chain reinvention and project-based cost initiatives like Project Energize, which aimed to offset gross margin pressures from raw material inflation and logistics volatility. In the first half of 2025, adjusted gross profit fell 12.8% in Q2 amid these dynamics, though organic sales growth held at low-single digits, signaling resilience in core categories. Key challenges included portfolio fragmentation and non-core asset drags, prompting a "Three-S" strategy—stabilize, streamline, and strengthen—initiated around 2023 to refocus on high-margin self-care products. This involved divesting the Dermacosmetics business in July 2025 for up to €327 million (expected close Q1 2026), which contributed to short-term sales declines like the 3.5% drop to $1.04 billion in Q1 2025 (3.2% from divestitures/exits). Regulatory hurdles in multi-market operations and supply chain vulnerabilities exacerbated earnings softness, but U.S.-centric manufacturing helped mitigate global disruptions. Perrigo reduced debt by repaying $400 million in senior notes in Q4 2024, lowering total debt to $3.62 billion, while reaffirming modest fiscal 2025 growth outlook (reported net sales 0-3%, organic 1.5-4.5%, skewed lower).

Tax Disputes and Strategies

Perrigo implemented a tax inversion strategy in 2013 by acquiring the Irish biotechnology firm Elan Corporation for $8.6 billion, which allowed the company to relocate its legal domicile to Ireland and benefit from the country's 12.5% corporate tax rate on trading income. This move reduced Perrigo's effective tax rate from 27.3% in fiscal 2013 to 24.7% in fiscal 2014, saving over $7 million in tax expense that year alone. The inversion exemplified broader corporate efforts to minimize U.S. tax exposure through foreign acquisitions, though it drew scrutiny amid U.S. legislative pushes to curb such restructurings. In parallel, Perrigo employed transfer pricing arrangements involving foreign subsidiaries to allocate intellectual property profits offshore. A key example involved the 2006 assignment of rights to the omeprazole patent (a generic version of Prilosec) to an Israeli affiliate, which licensed the technology back to U.S. operations, directing substantial income to lower-tax jurisdictions. The IRS audited Perrigo's 2007–2012 tax years, challenging the economic substance of the structure and reallocating over $500 million in income to U.S. entities under Section 482, resulting in $143 million in assessed taxes, penalties, and interest. Perrigo paid the amounts and filed refund claims, leading to litigation in the U.S. District Court for the Western District of Michigan. On September 25, 2025, the court largely ruled in Perrigo's favor, upholding the arm's-length nature of the pricing based on contemporaneous projections and rejecting the IRS's invocation of the economic substance doctrine to override transfer pricing rules. The decision awarded Perrigo a $163 million refund and permitted deduction of related litigation expenses, marking a significant setback for IRS efforts to apply economic substance penalties in transfer pricing contexts. This outcome affirmed that documented business purposes and comparable uncontrolled pricing could prevail over post-hoc IRS assertions of artificiality, even where actual profits exceeded projections. Perrigo also faced disputes with Irish tax authorities over the classification of proceeds from the 2016 sale of Tysabri patent rights to Biogen for $7.2 billion. Perrigo reported the gains as trading income eligible for Ireland's 12.5% rate, but the Irish Revenue Commissioners issued a €1.64 billion assessment in 2018, treating portions as non-trading capital gains taxed at 33%. After negotiations, Perrigo settled in September 2021 for €297 million (approximately $350 million), incorporating credits and offsets for a net cash outlay of €266.1 million, resolving all related liabilities without admission of wrongdoing. This settlement applied an alternative computational basis, avoiding prolonged litigation while preserving Perrigo's overall low-tax structure post-inversion.

Regulatory and Product Safety Issues

In August 2023, the U.S. Food and Drug Administration (FDA) issued a warning letter to Perrigo Wisconsin, LLC, citing significant violations of current good manufacturing practice (CGMP) regulations under 21 CFR Part 106 at its Gateway facility in Beloit, Wisconsin, which manufactures infant formula. The letter highlighted failures including inadequate investigation of Cronobacter contamination in finished products on multiple occasions, insufficient environmental monitoring for pathogens, and lack of corrective actions to prevent recurrence, contributing to broader concerns over infant formula quality control amid the 2022 U.S. shortage. Perrigo has conducted multiple voluntary recalls of infant formula products due to microbial and nutritional safety risks. In March 2023, the company recalled certain lots of Gerber Good Start SoothePro Powdered Infant Formula produced at the Gateway facility over potential Cronobacter sakazakii contamination, a bacterium linked to severe infections in infants; this followed internal testing and was not tied to consumer illnesses but prompted enhanced FDA scrutiny. In June 2019, Perrigo recalled 35-ounce containers of Parent's Choice Advantage Infant Formula Milk-Based Powder with Iron due to low levels of vitamin C, posing risks of nutritional deficiency. Additionally, in August 2024, Perrigo initiated a recall of one batch of Premium Infant Formula with Iron Milk-Based Powder because of elevated vitamin D levels, which could lead to toxicity including hypercalcemia in infants if consumed long-term. Beyond microbial and nutritional concerns, Perrigo faced regulatory action over heavy metal contaminants in its store-brand infant and toddler formulas. In February 2022, the company settled a 2018 lawsuit filed by California's Attorney General and a coalition of district attorneys, agreeing to limit lead levels to a target of 4 parts per billion (ppb) and a maximum of 10 ppb in products sold in California, while paying $72,500 in civil penalties; the suit stemmed from testing revealing elevated arsenic and lead posing cancer and developmental risks to children. Other product safety recalls include Perrigo's October 2019 worldwide voluntary recall of ranitidine products due to potential N-nitrosodimethylamine (NDMA) impurity, a probable human carcinogen above acceptable intake levels. In September 2020, the FDA alerted consumers to a voluntary recall of Perrigo's albuterol sulfate inhalation aerosol after reports of device clogging and inadequate medication delivery, manufactured by third-party Catalent Pharma Solutions. Earlier, in November 2013, Perrigo recalled infant acetaminophen drops nationwide due to potential risk of life-threatening overdosing from concentrated dosing errors. These incidents reflect ongoing challenges in ensuring compliance with FDA standards for over-the-counter and nutritional products.

Shareholder and Antitrust Litigation

In 2015, Mylan N.V. launched a hostile takeover bid for Perrigo Company plc, which Perrigo's board rejected, citing undervaluation and strategic concerns; shareholders subsequently filed a securities class action lawsuit alleging that Perrigo and its officers, including CEO Joseph C. Papa, made false and misleading statements about the company's financial health and takeover defenses, artificially inflating stock prices during the class period from April 21, 2015, to May 2, 2017. The suit claimed these misrepresentations led to investor losses when the takeover failed and Perrigo's stock declined amid revealed operational challenges, such as inventory issues and earnings shortfalls. In April 2024, the U.S. District Court for the District of New Jersey approved a $97 million cash settlement, with Perrigo denying wrongdoing but agreeing to resolve claims to avoid further costs; the settlement covered certified classes of shareholders, marking one of the larger recoveries in similar takeover-related securities disputes. A related dispute arose when certain institutional investors attempted to opt out of the class settlement to pursue individual claims but failed to file timely notices, leading to a 2025 Third Circuit Court of Appeals ruling upholding the district court's denial of their motion to vacate the opt-out deadline; the court cited the investors' procedural errors, preventing revival of their separate suit against Perrigo officers for alleged breaches tied to the Mylan bid resistance. On the antitrust front, Perrigo faced a 2023 Third Circuit decision in its suit against AbbVie Inc., where claims of anticompetitive delay in generic drug launches via sham patent litigation were barred by a prior 2012 settlement release covering pre-March 27, 2012, conduct; the ruling emphasized accrual of antitrust injury post-release, limiting Perrigo's recovery for alleged market exclusion in generic versions of AbbVie's TriCor. Separately, in February 2024, a U.S. District Court in Massachusetts denied Perrigo's motion to dismiss an antitrust suit by distributor P&L Associates, alleging Perrigo conspired with Gerber Products Company to restrict store-brand infant formula competition by limiting Gerber's entry into private-label production, thereby maintaining supracompetitive pricing; the court found plausible motives and effects under Sherman Act Section 1, allowing the case to proceed. Perrigo has denied the conspiracy claims, asserting independent business decisions. Earlier, Perrigo resolved state-led antitrust claims in a multistate milk pricing investigation with a $1 million settlement in 2020, contributing to a broader fund without admitting liability.

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