CPAP

In June 2021, Philips initiated a recall of millions of these machines after identifying degradation of the polyester-based polyurethane (PE-PUR) foam component, potentially leading to the release of toxic and carcinogenic particles and gases. This recall and the subsequent legal fallout have made headlines, drawing the attention of lawyers, investors, and affected patients.

As of March 2023, Philips faces 436 federal lawsuits consolidated under Senior U.S. District Judge Joy Flowers Conti in Pittsburgh by the Judicial Panel on Multidistrict Litigation (JPML). The first consolidation occurred in October 2021 with over 110 federal CPAP lawsuits. Furthermore, Philips confronts several class action lawsuits for financial damages.

The lawsuits allege that Philips knew or should have known about the risks associated with the PE-PUR foam but failed to warn patients or the medical community. Many patients allege suffering from cancer, lung problems, and other injuries due to the use of these recalled devices.

As this is an active litigation, there have been no settlements or jury verdicts yet. The plaintiffs propose to initiate bellwether trials as early as 2024, but the defendants are lobbying for a schedule that would push the first trial to 2025 or 2026.

As the number of cases is expected to grow, reaching over 1,000 by the end of 2023, the Philips CPAP lawsuit remains a key focus for the legal community and investors. The situation is continually evolving, with all parties closely monitoring the developments. This litigation highlights the critical need for manufacturers to ensure the safety of their products and the necessity for stringent checks and balances in the healthcare industry. The progress made so far underscores the importance of legal recourse in the quest for justice and compensation for affected patients.