Philips Piles on Another Trio of Class I Recalls for Beleaguered Ventilator Portfolio
Philips is facing another string of recalls in its portfolio, which have a received a Class I rating, the most serious type of recall.
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Thousands of Ventilators Pulled as Electrical Faults Put UK Patients’ Lives at Risk
Amid an ongoing current of medical product recalls, hospitals in the United Kingdom are experiencing new electrical problems with certain Philips ventilators.
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Philips’ Ventilator Woes Drag on with Yet Another Class I Recall
The U.S. FDA announced a Class I recall—the most serious type of recall—for the Philips Respironics V60 and V60 Plus Ventilator.
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FDA Orders Philips to Notify Patients of Recall of Certain Breathing Assistance Machines
The FDA issued a notification order to Philips Respironics requiring the company to of the recall of certain breathing assistance machines.
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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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