Man Waiting Months for BiPap Machine to Be Fixed After Recall
Complications involving a recall for certain sleep and respiratory care devices are causing some to make difficult personal health decisions.
Read MoreComplications involving a recall for certain sleep and respiratory care devices are causing some to make difficult personal health decisions.
Read MoreDec 29, 2021 | Company News, Recalls | 0 |
Philips Respironics has been conducting comprehensive testing to address potential health risks related to the PE-PUR sound abatement foam in the devices.
Read MoreDec 13, 2021 | Recalls, Ventilators | 0 |
Philips and U.S. regulators are continuing discussions on an earlier recall of its ventilators, where parts being used contained potentially hazardous foam.
Read MoreNov 24, 2021 | Recalls, Ventilators | 0 |
Philips is scrutinizing a recall of its ventilators and respiratory devices from the U.S. FDA.
Read MoreNov 17, 2021 | FDA Updates, Recalls | 0 |
Despite Philips getting the green light from the U.S. FDA to start repairing and replacing ventilators impacted by the company’s class 1 recall, the FDA exposed a possible safety risk concerning a replacement component.
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