Philips Was Correct In Disputed Death Reports, FDA Confirms

Last month, the US FDA increased the number of injuries and deaths initially reported in a March recall from Philips, which the company disputed. The FDA now says its adjusted numbers were in error.

Correction
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Earlier this month, Medtech Insight reported a dispute between the Food and Drug Administration and Philips over the number of injuries and deaths linked to a recall of the company’s breathing machines.

The question centered around a March recall of 100,000 Philips BiPAP A30, BiPAP A40, BiPAP V30, and OmniLab Advanced Plus...

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