WebbOn June 14, Philips issued a recall for many of its CPAP, BiPAP and ventilator machines because of concerns that users may inhale small particles of the foam used to dampen sound while the machines are in use. The recall notes that the foam may degrade over time and may also emit at least two harmful toxins. Webb25 jan. 2024 · This Philips Respironics December 2024 update is intended to provide healthcare providers, patients, and other stakeholders with updated information on the …
Recall: Philips Breathing Devices for Health Risks - WebMD
Webb10 apr. 2024 · Credit: The U.S. Food and Drug Administration. Sleep and home respiratory care products provider Philips Respironics (Philips) is recalling certain reworked DreamStation devices due to the risk of delivering inaccurate or insufficient therapy. The company began the recall of 1,088 devices in the US in February this year. Webb10 apr. 2024 · The FDA has tracked complaints numbering 98,000 since the 2024 recall. People have reported having respiratory problems, pneumonia, dizziness, chest pain, infections and cancer. In addition, the ... poly wet/dry vac
Philips provides update on the test and research program in
Webb12 apr. 2024 · If you registered a first-generation DreamStation CPAP, BiPAP Pro or Auto BiPAP device, we may need your device prescription and are unable to ship your … Webb12 apr. 2024 · April 12, 2024. Phillips has recalled more than 1,000 reworked Respironics DreamStation CPAP, BiPAP machines. The machines, which were initially recalled in June 2024, still may not be working properly. In a statement posted on the Food and Drug Administration's website, Phillips says the machines were assigned duplicate or … Webb15 juli 2024 · Medical equipment maker Philips is facing a raft of lawsuits following the announcement last month that it was recalling about 2 million machines used by obstructive sleep apnea patients in the US. polywhale