FDASeptember 19, 2018device

Philips DigitalDiagnost software 4.1.x and 4.2.x, A Stationary X-ray System Models: 712027, 712028, 712029, 712031, 712032701032, 712033, 712224, 712225, 712226, 712227, 712228.

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

The hazard

Stitching run on SkyPlate detector interrupted intermittently; Stitching with SkyPlate aborts after first image; System software CD contains wrong baseline

What to do

FDA enforcement status: Terminated

Brands named

philips medical systems gmbh dmcphilipsphilips medical

UPCs

712032701032

Recall history

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

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