FDANovember 7, 2018device

Stationary Fluoroscopic X-ray System CombiDiagnost R90, Model 709030 Stationary Fluoroscopic X-ray System

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

The hazard

kV/mA lockin not functioning as specified which may result in the patient receiving an increased radiation dose.

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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