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FDAJuly 19, 2016device

UroDiagnost; x-ray system. Product Code: 708033

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

The hazard

The two bolts that attach the clamping plate to the lateral shaft may break, which could cause the c-arm to move laterally forward, slide out of its bearings, and sag

What to do

FDA enforcement status: Terminated

Brands named

philips electronics north americaphilipsphilips electronics

Recall history

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

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