US federal court orders Philips Respironics to restrict CPAP & BiPAP machine production/sale, implement recall remediation, and offer compensation due to FDA concerns.
US federal court entered a consent decree against Philips Respironics, restricting the production and sale of CPAP & BiPAP machines at several US facilities over recall concerns. The FDA requires Philips to implement a recall remediation plan, ensuring consumers are compensated with new, reworked, or remediated devices, or partial refunds. The decree aims to prioritize patient relief and ensure compliance.
April 09, 2024
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