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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NotiSphere has been awarded a contract with Vizient for its recall management solution, allowing suppliers to share product alerts.
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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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Recalls for medical devices declined in 2021, though details surrounding the decline are not as clear cut as the final data may suggest.
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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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