Mealey's Drugs & Devices

  • May 01, 2024

    Oklahoma Federal Judge Dismisses Some Claims In Underfilled Drug Vial Cases

    OKLAHOMA CITY — The Oklahoma federal judge overseeing cases involving claims that a company underfilled vials of the breast cancer drug Herceptin found that the plaintiffs have not stated a claim for relief under California’s unfair competition law (UCL) and false advertising law (FAL) and dismissed those claims.

  • April 30, 2024

    Bard Denies Claims Made By Woman Alleging Defective IVC Filter Caused Damage

    SEATTLE — C.R. Bard Inc. and Bard Peripheral Vascular Inc. filed an answer to a woman’s complaint in a Washington federal court, denying her allegations that its inferior vena cava (IVC) filter was defective and caused her significant injuries.

  • April 30, 2024

    Insulin Manufacturers, PBMs Hit With RICO Suit Alleging Conspiracy

    HARTFORD, Conn. — A union health benefit plan sued the top three insulin manufacturers and a host of pharmacy benefit managers (PBMs) in a Connecticut federal court, alleging that they conspired to artificially inflate the price of the prescription drug in violation of the Racketeer Influenced and Corrupt Organizations Act (RICO).

  • April 29, 2024

    Publix: Georgia County Misses Point Of Motion To Certify Questions In Opioid Case

    CLEVELAND — Publix Super Markets Inc. says Cobb County, Ga.’s opposition to its motion to certify to the Georgia Supreme Court a series of questions for the high court to determine how the state’s public nuisance law applies in the opioid multidistrict litigation actually demonstrates the need for the high court to weigh in.

  • April 29, 2024

    Hernia Mesh MDL Judge OKs Dismissal Of 28 Cases After Agreements Reached

    ATLANTA — The judge overseeing the Ethicon Physiomesh hernia patch multidistrict litigation granted a motion to dismiss with prejudice 28 cases after the parties told the court in a joint motion that they have settled all claims in those cases.

  • April 29, 2024

    CPAP MDL Parties Reach $1.1B Settlement To End Injury, Medical Monitoring Claims

    PITTSBURGH — Philips Respironics and the plaintiffs in the multidistrict litigation involving personal injuries caused by deteriorating sound insulation in Philips’ continuous positive airway pressure (CPAP) devices, which led to a recall of approximately 10.8 million sleep apnea devices, on April 29 announced an agreement for $1.1 billion to settle all personal injury claims and the medical monitoring class action.

  • April 26, 2024

    MDL Judge Grants Final Approval To Economic Claims Settlement For CPAP Devices

    PITTSBURGH — The federal judge overseeing the multidistrict litigation involving the recall of approximately 10.8 million continuous positive air pressure (CPAP) sleep apnea devices on April 25 granted final approval of a $506 million settlement to end all economic claims in addition to an award of $95 million for attorney fees and costs in connection with the settlement.

  • April 26, 2024

    Indivior Proposes Plan For Phased Discovery In Suboxone MDL

    CLEVELAND — Indivior Inc., a defendant in the Suboxonefilm multidistrict litigation, filed a supplemental proposal for phased discovery on general causation following a request from the judge overseeing the MDL during a conference meeting.

  • April 26, 2024

    CGL Insurer Dismissed From Coverage Dispute Arising From Opioid Epidemic

    SPARTANBURG, S.C. — Parties filed a stipulation in a South Carolina federal court dismissing one commercial general liability insurer without prejudice from the insurers’ lawsuit seeking a declaration that they have no duty to defend or indemnify against governmental entities’ underlying lawsuits alleging that their insured caused or contributed to the opioid crisis by improperly marketing, distributing and selling opioid medications.

  • April 25, 2024

    Diabetes And Diet Drug MDL Names Co-Lead Counsel, Plaintiffs’ Committee Members

    PHILADELPHIA — The federal judge overseeing the multidistrict litigation involving diabetes and diet drugs that consumers allege caused gastrointestinal and other injuries appointed counsel to lead the plaintiffs.

  • April 25, 2024

    Pharmaceutical Company Says FDA’s Approval Of Generic Drug Violated FDCA

    WASHINGTON, D.C. — A pharmaceutical company moved for summary judgment in its suit against the U.S. Food and Drug Administration, asking a federal judge in the District of Columbia to order that the FDA vacate its approval of the abbreviated new drug application (ANDA) for generic tasimelteon and recall the drug.

  • April 23, 2024

    Judge Adopts Magistrate’s Recommendation To Deny Motion To Amend Taxotere Complaint

    NEW YORK — A New York federal magistrate judge’s report and recommendation denying a motion to amend a complaint is “supported by the already vast body of case law denying Taxotere plaintiffs’ motions to amend,” a federal judge said in adopting the report.

  • April 23, 2024

    SoClean Says MDL’s Plan For Third-Party Complaints Violates Federal Rules

    PITTSBURGH — A manufacturer of equipment that uses ozone to clean or disinfect medical devices and accessories objected to a special discovery master’s report and recommendation filed in a multidistrict litigation involving the recall of approximately 10.8 million Philips continuous positive air pressure (CPAP) sleep apnea devices and respirators, arguing that the procedures outlined for handling third-party litigation are inadequate.

  • April 22, 2024

    Walgreens To Pay $110 Million To Philadelphia For Role In City’s Opioid Crisis

    PHILADELPHIA — Philadelphia announced April 19 that it has reached a $110 million settlement with Walgreen Co. to settle claims that its failure to monitor suspicious opioid prescriptions or ensure that it dispensed opioid pain medications for a legitimate medical purpose caused harm to the city.

  • April 19, 2024

    Endo Health Pleads Guilty In Michigan Federal Court To Mislabeling Opioid Drug

    DETROIT — Endo Health Solutions Inc. (EHSI) on April 18 pleaded guilty in a Michigan federal court to violating the Food, Drug and Cosmetic Act (FDCA) by marketing its opioid drug Opana ER as crush and tamper resistance.

  • April 18, 2024

    Mass Tort Cases For Drugs, Medical Devices

    New developments in the following mass tort drug and device cases are marked in boldface type.

  • April 18, 2024

    Federal Circuit Defines ‘Surgical Intervention’ In Vaccine Injury Act Appeal

    WASHINGTON, D.C. — The Federal Circuit U.S. Court of Appeals found that a lower court “relied upon a legally erroneous construction of ‘surgical intervention’” and reversed and remanded a decision that a claim was ineligible for compensation under the National Childhood Vaccine Injury Act.

  • April 17, 2024

    Settlement With Eli Lilly Over Insulin Costs Falls Apart In National Class Action

    NEWARK, N.J. — A proposed settlement between Eli Lilly & Co. and class members in which the drugmaker would pay $13.5 million for an insulin price claims fund and ensure that class members will have prices for certain Lilly insulins capped at $35 a month for four years is off the table, lawyers for the plaintiffs told a New Jersey federal judge.

  • April 17, 2024

    Taxotere MDL Judge Denies Motions For Reconsideration Of Dismissed Cases

    NEW ORLEANS — The Louisiana federal judge overseeing the Taxotere hair loss multidistrict litigation denied 10 motions for reconsideration filed by plaintiffs whose cases were dismissed for failure to comply with a court-ordered deadline to properly serve their complaints.

  • April 17, 2024

    FDA Recalls Heart Devices Linked To Injuries, Death

    SILVER SPRING, Md. — The U.S. Food and Drug Administration has announced a recall of nearly 14,000 HeartMate II and HeartMate 3 Left Ventricular Assist System (LVAS), citing reports that buildup in components can obstruct the device and make it less effective in helping the heart pump blood.

  • April 17, 2024

    Plaintiffs In ASD-ADHD MDL Appeal Judgment, Exclusion Of Experts To 2nd Circuit

    NEW YORK — Plaintiffs in the acetaminophen autism spectrum disorder-attention deficit hyperactivity disorder (ASD-ADHD) multidistrict litigation who allege that prenatal exposure to acetaminophen causes autism or attention deficit hyperactivity disorder have appealed to the Second Circuit U.S. Court of Appeals a decision by the MDL judge to exclude their expert witnesses and to enter final judgment dismissing their cases.

  • April 17, 2024

    Deadlines For 1st Bellwether Trials In Covidien Hernia Mesh MDL Pushed Back

    BOSTON — The federal magistrate judge overseeing the multidistrict litigation involving Covidien hernia mesh agreed to extend dates in the current scheduling order by eight months after the plaintiffs cited “significant discovery deficiencies” on the part of the defendants.

  • April 16, 2024

    High Court Declines Woman’s Request To Review Lactaid Labeling Claim Dismissal

    WASHINGTON, D.C. — The U.S. Supreme Court on April 15 denied woman’s petition to review a First Circuit U.S. Court of Appeals ruling that her claims that she was misled into purchasing Lactaid products are preempted by the U.S. Food and Drug Administration’s statutory enforcement authority under the Food, Drug and Cosmetic Act (FDCA).

  • April 15, 2024

    JPMDL Won’t Transfer Hawaii Drug Pricing Suit To Insulin Pricing MDL

    WASHINGTON, D.C. — The Judicial Panel on Multidistrict Litigation (JPMDL) refused to transfer a case pending in a Hawaii federal court in which the state alleges “a scheme to inflate the list price of all ‘brand-name prescription drugs’ — a substantially larger universe of drugs, manufacturers, and business practices than those at issue in the MDL” that centralized federal insulin pricing lawsuits.

  • April 15, 2024

    JPMDL: OTC Cold Medicine MDL Will Include Maximum Strength Label Cases

    WASHINGTON, D.C. — The Judicial Panel on Multidistrict Litigation (JPMDL) agreed to transfer cases involving “Maximum Strength” labeling on over-the-counter cough and cold medications containing the active ingredient phenylephrine (PE) to the multidistrict litigation for cases alleging that the medications are ineffective at relieving nasal congestion.

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