U.S. FDA Labels Philips Expanded Ventilator Recall as Most Serious
Certain Philips ventilators that were recalled last year may lead to injuries or death, according to a new classification of the recall by the FDA.
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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.
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Philips Provides Update on Sleep Care Product Recall
Philips Respironics has been conducting comprehensive testing to address potential health risks related to the PE-PUR sound abatement foam in the devices.
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Philips in Talks with FDA After New Ventilator Findings
Philips and U.S. regulators are continuing discussions on an earlier recall of its ventilators, where parts being used contained potentially hazardous foam.
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Philips Investigates Number of Complaints in FDA Ventilator Report
Philips is scrutinizing a recall of its ventilators and respiratory devices from the U.S. FDA.
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