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FDA classifies Baxter's hospital bed system recall as most serious

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The U.S. health regulator on Wednesday classified the recall of hospital bed systems by Baxter International Inc , as the most serious type, on concerns it could lead to life-threatening injuries or death.

Signage is seen outside of the Food and Drug Administration headquarters in White Oak, Maryland, U.S., August 29, 2020. REUTERS/Andrew Kelly/File Photo

In the letter, Baxter warned users about the potential for WatchCare's radio frequencies to interfere with other medical devices. The correction letter was updated last month to include actions healthcare practitioners could undertake in case they encountered any malfunction or interference. Baxter, which makes smart hospital beds, recalled 8,550 WatchCare devices distributed between Aug. 1, 2018 and Sept. 1, 2022.

 

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