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FDADecember 2, 2021device

Zenition 50, Model #718096

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Firm discovered that the wireless foot switch can suddenly stop responding due to a firmware issue. If the wireless foot switch fails, there could be a delay or interruption of procedure if the hand switch is not used or if the wired foot switch is not connected to the system.

What to do

FDA enforcement status: Ongoing

Brands named

philips medical systems nederland b vphilipsphilips medical

UPCs

459801238191459801238231

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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