Mealey's Drugs & Devices

  • February 15, 2024

    Mass Tort Cases For Drugs, Medical Devices

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

  • February 15, 2024

    Gardasil Vaccine MDL Reassigned To Judge Bell In Western District Of N.C.

    WASHINGTON, D.C. — The Gardasil vaccine multidistrict litigation has been reassigned to U.S. Judge Kenneth D. Bell of the Western District of North Carolina, the chair of the U.S. Judicial Panel on Multidistrict Litigation (JPMDL) announced in a one-page order.

  • February 15, 2024

    Arizona Federal Judge Grants Final Approval In Theranos Suit Against Walmart

    PHOENIX — An Arizona federal judge has entered final approval of a $44 million settlement agreement with pharmacy chain Walgreens to resolve class claims involving tests conducted in Arizona and California pharmacies by the now-defunct Theranos Inc. blood testing company.

  • February 14, 2024

    6th Circuit Finds No Error In Expert Exclusion That Ended Onglyza MDL

    CINCINNATI — The federal judge presiding over the Onglyza multidistrict litigation “had three good reasons to find” that testimony by an expert retained to opine that the drug is capable of causing heart failure was inadmissible, a Sixth Circuit U.S. Court of Appeals panel said Feb. 13, affirming the final judgment entered in the case.

  • February 14, 2024

    Fla. Federal Judge Gives Woman 1 Last Chance To Amend Defective Hip Complaint

    FORT MYERS, Fla. — A federal judge in Florida on Feb. 13 granted a woman one final attempt to amend her complaint to separate any commingled strict liability failure to warn claim from the negligence claim in a defective “metal-on-metal” hip replacement device case.

  • February 13, 2024

    Amended Master Personal Injury Complaint Filed Under Seal In CPAP MDL

    PITTSBURGH — Plaintiffs in the multidistrict litigation involving the recall of approximately 10.8 million Philips continuous positive air pressure (CPAP) sleep apnea devices and respirators on Feb. 12 filed under seal a second amended master long-form complaint for personal injuries after the Pennsylvania federal judge overseeing the case in January adopted in part recommendations from the special master and dismissed certain claims with leave to amend.

  • February 13, 2024

    Lilly Agrees To Cap Insulin Costs At $35 In Minnesota Settlement Agreement

    NEWARK, N.J. — Eli Lilly and Co. has agreed to make its insulin products available to consumers in Minnesota for no more than $35 for a monthly subscription as part of a settlement agreement reached with the state.

  • February 13, 2024

    JPMDL Rejects Objections To Transfer Of 3 Cases In Bard Port Catheter MDL

    WASHINGTON, D.C. — The U.S. Judicial Panel on Multidistrict Litigation (JPMDL) denied a motion filed by a port catheter device maker to vacate two conditional transfer orders, rejecting its argument that including a trio of complaints “would expand the scope” of the multidistrict litigation.

  • February 13, 2024

    Judge Grants Summary Judgment In Taxotere Case, Says Woman On Notice Of Injury

    PEORIA, Ill. — An Illinois federal judge found that a woman was on notice that Taxotere, a chemotherapy used to treat breast cancer, was the possible cause of her permanent hair loss and that her complaint was filed after the statute of limitations expired.

  • February 12, 2024

    Insured Seeks Rehearing, Certification Of Questions In Opioid Coverage Dispute

    SAN FRANCISCO — A prescription drug distributor insured on Feb. 9 asked the Ninth Circuit U.S. Court of Appeals to reconsider its ruling that there is no coverage owed for underlying lawsuits prompted by the opioid epidemic because the underlying claims “describe exclusively deliberate conduct,” arguing that a panel rehearing or rehearing en banc is warranted so the panel can certify two “undecided, critical questions of California law” to the California Supreme Court.

  • February 09, 2024

    Mifepristone Maker Argues W.Va.’s Law On Abortion Conflicts With Federal Law

    RICHMOND, Va. —The West Virginia Unborn Child Protection Act (UCPA), which bans abortion in almost all cases, is preempted under federal law because Congress has made it clear that only the U.S. Food and Drug Administration may determine “which restrictions are necessary to ensure mifepristone’s safe use while minimizing burdens,” GenBioPro Inc., the maker of generic mifepristone, tells the Fourth Circuit U.S. Court of Appeals in its opening brief.

  • February 09, 2024

    Defective Medical Device Suit Partially Dismissed In Alabama Federal Court

    MONTGOMERY, Ala. — An Alabama federal judge on Feb. 7 granted a manufacturer’s partial motion to dismiss a complaint filed by a man who alleges that a vascular access device used during chemotherapy was defective.

  • February 08, 2024

    Man Alleges Defect In Da Vinci Robot Device Led To His Wife’s Death

    WEST PALM BEACH, Fla. — A man sued the manufacturer of the da Vinci robot in a Florida federal court, alleging that it concealed a defect in the multiarmed, remote controlled surgical device that caused a small cut in his wife’s intestines that led to her death.

  • February 07, 2024

    FDA, Danco Oppose States’ Intervention In Abortion Drug Case In High Court

    WASHINGTON, D.C. — Three anti-abortion states on Feb. 6 replied to oppositions filed by the U.S. Food and Drug Administration and by Danco Laboratories LLC, the manufacturer of Mifeprex-brand mifepristone, on the states’ motion to intervene in a U.S. Supreme Court case involving the abortion drug with the FDA arguing “that the states waited far too long to seek intervention.”

  • February 07, 2024

    SoClean Moves To Dismiss Countersuit By Philips In Foam Degradation Dispute

    PITTSBURGH — SoClean Inc., which sells machines that use ozone to clean and disinfect CPAP devices and accessories, asks a Pennsylvania federal court to dismiss counterclaims filed by Koninklijke Philips NV and its affiliates that allege that SoClean’s sale of the products violated federal law.

  • February 06, 2024

    Hernia Mesh MDL Judge Cancels Plans For 4th Bellwether Trial, Denies Remand

    COLUMBUS, Ohio — The Ohio federal judge overseeing the Davol hernia mesh multidistrict litigation said the “usefulness of another lengthy and expensive trial is dubious at best” and vacated the scheduling order for the fourth bellwether trial but denied a motion by the plaintiffs to begin the remand process.

  • February 06, 2024

    JPMDL Centralizes Suboxone Cases In Northern District Of Ohio

    WASHINGTON, D.C. — The U.S. Judicial Panel on Multidistrict Litigation (JPMDL) agreed that cases alleging that Suboxone film, a prescription drug used to treat opioid use disorder, causes extensive dental decay involve common question of facts and ordered the cases to be centralized in the U.S. District Court for the Northern District of Ohio before Judge J. Philip Calabrese.

  • February 06, 2024

    JPMDL Centralizes Diabetes Drug Cases In Eastern District Of Pennsylvania

    WASHINGTON, D.C. — The Judicial Panel on Multidistrict Litigation (JPMDL) agreed to centralize cases alleging that diabetes and diet drugs caused consumers to suffer gastrointestinal and other injuries and assigned the multidistrict litigation to Judge Gene E.K. Pratter of the U.S. District Court for the Eastern District of Pennsylvania.

  • February 05, 2024

    New Plaintiffs In ASD-ADHD MDL Argue Their Expert Can Prove Causation

    NEW YORK — A group of plaintiffs who allege that prenatal exposure to acetaminophen causes autism (ASD) or attention deficit hyperactivity disorder (ADHD) responded to an order from the judge overseeing the multidistrict litigation, arguing that because their cases were filed after she ruled that general causation experts are inadmissible under Federal Rule of Evidence 702, they should be allowed to present their own experts.

  • February 05, 2024

    FDA: 111 More Deaths Reportedly Connected To Philips CPAP Devices

    SILVER SPRING, Md. — The U.S. Food and Drug Administration released an update on medical device reports (MDRs) associated with the alleged breakdown of polyester-based polyurethane (PE-PUR) foam used in continuous positive air pressure (CPAP) devices, bi-level positive air pressure (Bi-PAP) devices and ventilators made by Philips Respironics, noting that 111 additional deaths have been reported.

  • February 05, 2024

    Hikma, Ad Agency Reach Settlements For Role In Opioid Crisis

    NEW YORK — Hikma Pharmaceuticals has agreed to a $150 million multistate settlement for its role in the opioid epidemic, New York Attorney General Letitia James announced on behalf of the participating states; the attorney general also announced a separate $350 million settlement that resolves allegations that Publicis Health LLC, an advertising agency working with Purdue Pharma LP, “helped create and maintain a public nuisance.”

  • February 01, 2024

    Mass Tort Cases For Drugs, Medical Devices

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

  • February 01, 2024

    CPAP MDL Judge Allows Plaintiffs To File Amended Master Personal Injury Complaint

    PITTSBURGH — The federal judge overseeing the multidistrict litigation involving the recall of approximately 10.8 million Philips continuous positive air pressure (CPAP) sleep apnea devices and respirators has adopted and rejected certain recommendations from the special master and granted a motion to allow the plaintiffs to modify the master complaint for personal injuries (master PI complaint).

  • February 01, 2024

    Judge Allows 3rd Amended Complaint To Proceed In Defective Hip Device Case

    FRANKFORT, Ky. — A Kentucky federal judge denied a “metal-on-metal” hip replacement device maker’s motion to dismiss a third amended complaint alleging injuries caused by a defective design.

  • February 01, 2024

    EBay Agrees To $59M Settlement For CSA Violation In Pill Press Machine Sales

    WASHINGTON, D.C. — The U.S. Department of Justice announced Jan. 31 that eBay Inc. will pay $59 million to settle allegations that it violated the Controlled Substances Act (CSA) by selling thousands of pill presses and encapsulating machines through its website.

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