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FDA (Device enforcement)Recalled 2023-12-15class i

Philips North America: BrightView, gamma camera system; Model Nos.: 6-digit format 882480; 12-digit format 453560279781 453560279791 453560279811 453560279801; 4x4 digit format 2170-3000A 2170-3001A 2

Hazard

Detector may unexpectedly fall due to a component failure. If the detector is positioned below center of gantry, there is a potential for abrasion, contusion, laceration, and/or fracture to the patient's lower limbs, as well as an interruption to normal system operation. If detector is positioned above center of gantry, there may be an interruption to normal system operation.

Details from the source

Reason for recall: Detector may unexpectedly fall due to a component failure. If the detector is positioned below center of gantry, there is a potential for abrasion, contusion, laceration, and/or fracture to the patient's lower limbs, as well as an interruption to normal system operation. If detector is positioned above center of gantry, there may be an interruption to normal system operation. Distribution: Domestic distribution nationwide. International distribution worldwide. Quantity: 302 US; 264 OUS Lot/code info: All serial numbers are affected. No UDI-DI available for this product.

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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