FDADecember 17, 2015device

BrightView are gamma cameras; Designed for single or dual detector nuclear imaging.

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

The hazard

The firm discovered four issues with the BrightView Family systems. Issue 1: During a cardiac non-Auto Body Contouring (ABC) scan, using Cardiac High Resolution (CHR) collimators, the collimator may come in contact with the bottom edge of the patient pallet. If this occurs, collision sensors would pause the scan. Issue 2: During a scan, the gantry motion may halt prematurely. This cause

What to do

FDA enforcement status: Terminated

Brands named

philips medical systems clevelandphilipsphilips medical

UPCs

4000703000340007050005400070600084000706000640007060007

Recall history

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

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BrightView are gamma cameras; Designed for single or dual detector nuclear imaging. — Recall Details · AllClear