Mealey's Drugs & Devices

  • January 02, 2024

    McKinsey To Pay $78 Million To Settle Third-Party Payers’ Claims In MDL

    SAN FRANCISCO — McKinsey & Co. Inc. has agreed to pay $78 million to settle claims from third-party payers (TPP) in an opioid multidistrict litigation.

  • December 22, 2023

    Zantac Maker, Retailer: Petition Does Not Address Question On Circuit Split

    WASHINGTON, D.C. — The manufacturer of Zantac and a retailer in a Dec. 21 opposition brief tell the U.S. Supreme Court that it should deny a petition for a writ of certiorari filed by a woman appealing the dismissal of her case and asking the high court to settle a jurisdictional question that has split the circuit courts because the “‘question presented’ is not actually presented in this case.”

  • December 22, 2023

    JPMDL Schedules Hearing To Decide On Creation Of Suboxone MDL

    WASHINGTON, D.C. — The U.S. Judicial Panel on Multidistrict Litigation will meet in Santa Barbara, Calif., on Jan. 25 to decide, among other petitions, whether to consolidate for pretrial purposes cases that allege that Suboxone film, a prescription drug used to treat opioid use disorder, causes extensive dental decay.

  • December 22, 2023

    Citing CPAP Recall, Senators Ask For Update On FDA’s Process On Oversight

    WASHINGTON, D.C. — Two senators sent a letter to the U.S. Government Accountability Office asking for an update to its 2011 report on “Medical Devices: FDA Should Enhance Its Oversight of Recalls” in light of the rising amount of recalls and adverse event reports, citing the recall of approximately 10.8 million Philips continuous positive air pressure (CPAP) sleep apnea devices and respirators.

  • December 21, 2023

    Louisiana Federal Judge Won’t Stay Diabetes Drug Case Pending MDL Decision

    LAKE CHARLES, La. — A Louisiana federal judge denied a motion filed by the manufacturer of Ozempic to stay proceedings while the parties await a decision on whether similar cases will be consolidated in a multidistrict litigation.

  • December 21, 2023

    JPMDL Hearing On Diabetes Drug MDL Scheduled; Deadline For Response Extended

    WASHINGTON, D.C. — The U.S. Judicial Panel for Multidistrict Litigation (JPMDL) granted a motion for an extension to respond to a motion filed by attorneys representing nine individuals who allege that they suffered gastrointestinal and other injuries from diabetes and diet drugs such as Ozempic, Wegovy and Mounjaro who want to transfer all currently filed and any subsequently filed cases and centralize them in the U.S. District Court for the Western District of Louisiana.

  • December 21, 2023

    Pa. Woman Accuses Ozempic Maker Of Deceptive Marketing Of Weight Loss Drug

    PHILADELPHIA — A woman alleges in a complaint in Pennsylvania federal court that she was injured as a result of a drug manufacturer’s “widespread, deceptive and unfair marketing” of Wegovy and Ozempic and through the use of the diabetes and weight loss drugs (Laura Marrero v. Novo Nordisk A/S, et al., No. 23-5036, E.D. Pa.).

  • December 20, 2023

    Amendments To Rule 702 For Expert Witness Testimony Go Into Effect

    Amendments to Federal Rule of Evidence 702, Fed. R. Evid. 702, went into effect to clarify how courts should decide the admissibility of expert testimony.

  • December 20, 2023

    Causation Experts Found Inadmissible In Acetaminophen Autism/ADHD MDL

    NEW YORK — The New York federal judge overseeing the acetaminophen autism spectrum disorder-attention deficit hyperactivity disorder (ASD-ADHD) multidistrict litigation found that the general causation experts retained by plaintiffs alleging that prenatal exposure to acetaminophen causes the disorders are inadmissible under Federal Rule of Evidence 702.

  • December 20, 2023

    1st Circuit Affirms Conviction, Fines For 2 Execs Convicted Of Off-Label Marketing

    BOSTON — The First Circuit U.S. Court of Appeals rejected arguments from former Acclarent Inc. executives who argued on appeal that their convictions for distributing and misbranding medical devices sold in interstate commerce violated the First Amendment to the U.S. Constitution and that the district court erred in its instructions to the jury.

  • December 19, 2023

    Health Care Tech Company Settles FCA Claims Over Heart Monitoring Fraud For $14.7M

    WASHINGTON, D.C. — The U.S. Department of Justice (DOJ) on Dec. 18 announced that BioTelemetry Inc. and its subsidiary LifeWatch Services Inc. have agreed to pay more than $14.7 million to resolve claims that they violated the federal False Claims Act (FCA) by knowingly submitting claims to government insurers for a higher level of remote cardiac monitoring than intended by physicians or that was medically necessary, resulting in higher reimbursements to LifeWatch.

  • December 19, 2023

    Excluded Expert Witness Can’t Testify As Fact Witness In Device Injury Case

    PHOENIX — A man alleging that a defective “metal-on-metal” hip replacement device caused an injury cannot present as a fact witness a person who has been excluded from testifying as an expert witness, an Arizona federal judge ruled, agreeing to strike his testimony.

  • December 14, 2023

    Judge Grants Manufacturer Summary Judgment In Remanded Prosthetic Shoulder Case

    NEW ORLEANS — A federal judge in Louisiana again awarded summary judgment to the manufacturer of a shoulder prosthesis after the case was remanded by the Fifth Circuit U.S. Court of Appeals, which vacated the previous summary judgment decision after finding that the question of whether the plaintiff’s claim had prescribed under Louisiana state law is “best left for the jury.”

  • December 14, 2023

    Mass Tort Cases For Drugs, Medical Devices

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

  • December 14, 2023

    Suboxone Film Manufacturers Agree That MDL Coordination Is Needed

    WASHINGTON, D.C. — The manufacturer of Suboxone film facing allegations that the prescription drug used to treats opioid use disorder caused extensive dental decay agreed in responses to a motion for transfer that the U.S. Judicial Panel on Multidistrict Litigation should consolidate the cases for pretrial purposes.

  • December 13, 2023

    Acetaminophen Autism/ADHD MDL Judge Renews Plaintiffs’ Leadership Team, Adds Members

    NEW YORK — The New York federal judge overseeing the acetaminophen autism spectrum disorder-attention deficit hyperactivity disorder (ASD-ADHD) multidistrict litigation has renewed and appointed members of the plaintiffs’ leadership team.

  • December 13, 2023

    High Court Agrees To Hear Dispute Over Abortion Drug Regulations

    WASHINGTON, D.C. — The U.S. Supreme Court will determine whether the Fifth Circuit U.S. Court of Appeals erred in upholding a district court’s stay of the Food and Drug Administration’s 2016 amendments to mifepristone’s approval and the agency’s 2021 decision not to enforce its regulations during the COVID-19 pandemic, the court announced Dec. 13, granting a petition for a writ of certiorari.

  • December 12, 2023

    Federal Magistrate Judge Recommends Partial Dismissal Of Surgical Mesh Injury Case

    SCRANTON, Pa. — A federal magistrate judge in Pennsylvania on Dec. 11 recommended partially granting a motion to dismiss filed by a surgical mesh manufacturer and its distributor facing claims that a man was injured after its product was used during surgery.

  • December 11, 2023

    Louisiana Federal Judge Allows Most Of Diabetes Drug Complaint To Move Forward

    LAKE CHARLES, La. — In separate orders, one signed Dec. 11 and another on Dec. 8, a Louisiana federal judge largely denied motions to dismiss filed by two drug manufacturers facing claims that a woman suffered gastrointestinal and other injuries after taking Ozempic and Mounjaro diabetes drugs.

  • December 11, 2023

    High Court Won’t Hear Appeal In Case Alleging Injury From CoolSculpting Procedure

    WASHINGTON, D.C. —The U.S. Supreme Court on Dec. 11 denied a petition for a writ of certiorari filed by a man who argued that an appellate court erred in granting summary judgment to the company that created the CoolSculpting process after finding that he was warned about the risk of paradoxical adipose hyperplasia (PAH) and that his design defect claims failed under the risk-utility or consumer expectations tests.

  • December 08, 2023

    Woman Says Manufacturer Knew Tepezza Could Cause Hearing Loss

    CHICAGO — A case alleging that the manufacturer of Tepezza, a prescription drug that treats thyroid eye disease, knowingly concealed information that the drug causes hearing loss has been assigned to U.S. Thomas M. Durkin in the U.S. District Court for the Northern District of Illinois, who ordered the parties to file a joint status report by Jan. 14.

  • December 08, 2023

    MDL Judge Transfers Last Of Testosterone Replacement Therapy Cases

    CHICAGO — The judge overseeing the testosterone replacement therapy (TRT) multidistrict litigation ordered that all remaining cases be transferred to other district courts, declaring that the “purposes of the MDL proceeding have been completed.”

  • December 08, 2023

    MDL Sought For Alleged Stomach Injuries From Diabetes, Diet Drugs

    WASHINGTON, D.C. — Attorneys representing nine individuals who allege that they suffered gastrointestinal and other injuries from diabetes and diet drugs such as Ozempic, Wegovy and Mounjaro have asked the U.S. Judicial Panel for Multidistrict Litigation (JPMDL) to transfer all currently filed and any subsequently filed cases and centralize them in the U.S. District Court for the Western District of Louisiana.

  • December 08, 2023

    Woman Sues CVS For Contaminated Eye Drops, Proposes Class Action

    WILMINGTON, N.C. — A woman filed a complaint in North Carolina federal court seeking to represent a class of consumers who purchased over-the-counter lubricating eyedrop products at CVS stores that were later recalled by the U.S. Food and Drug Administration.

  • December 07, 2023

    OTC Cold Medicine Cases Centralized In MDL Before Judge Cogan In New York

    WASHINGTON, D.C. — The Judicial Panel on Multidistrict Litigation on Dec. 6 agreed to centralize cases alleging that over-the-counter cough and cold medications containing the active ingredient phenylephrine (PE) are ineffective at relieving nasal congestion and assigned the multidistrict litigation to Judge Brian M. Cogan of the U.S. District Court for the Eastern District of New York.

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