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FDANovember 30, 2023device

BrightView X, Gamma Camera, Product Code 882478

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

The hazard

While using Pre-Programmed Motion during an extrinsic quality assurance scan, a gap is created between the patient support and the detector, which may present a potential extremity entrapment hazard. Risk to patients may include fracture, body part loss of function/debilitation, muscle or ligament sprain or strain, laceration, crush injury, abrasion, or contusion.

What to do

FDA enforcement status: Ongoing

Brands named

philips north americaphilipsphilips north

Recall history

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

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BrightView X, Gamma Camera, Product Code 882478 — Recall Details · AllClear