FDAJuly 22, 2020device

CombiDiagnost R90 Software Version R1.0 and R1.1

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

The hazard

Philips has become aware of a software issue, where the kV and mA values are not locked immediately but change when the collimator shutter position is changed directly after the Lock-In command. This software issue leads to an over or under exposed image.

What to do

FDA enforcement status: Ongoing

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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