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FDAJune 27, 2018device

DigitalDiagnost 4 High Performance (Stitching Patient Support) 712027

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

The hazard

The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.

What to do

FDA enforcement status: Terminated

Brands named

philips medical systems gmbh dmcphilipsphilips medical

Recall history

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

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