FDA Proposes Order Forcing Philips to Repair, Replace or Refund All Recalled Ventilators
The FDA is proposing an order be issued that would require Philips Respironics to address recalled devices, including millions of ventilators.
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Philips Investigates Reports of One Death, Four Injuries Potentially Tied to Ventilator Recall
Earlier this week, the U.S. FDA revealed that the Philips’ Respironics V60 ventilator received a Class 1 recall due to an electrical circuit fault that can use the device to malfunction. Now, Philips is investigating one patient death and four reports of patient harm possibly related to the recall.
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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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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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