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FDANovember 10, 2015device

Philips Healthcare DuraDiagnost stationary X-ray system

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

The hazard

The detector may signal that it is ready for acquisition when it actually is not, resulting in failure to properly acquire the X-ray image.

What to do

FDA enforcement status: Terminated

Brands named

philips healthcarephilips

Recall history

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

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