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Tag Archives: Medical Device Recall

FDA Report Reveals Inconsistencies In Philips Test Results

A massive Philips CPAP recall was issued earlier this year, impacting more than 15 million CPAP, BiPAP and ventilators that contained a polyester-based (PE-PUR) sound abatement foam, which was intended to reduce sounds and vibrations during use. However, the manufacturer now acknowledges that the CPAP foam degrades over time, and may release black particles or debris directly…