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FDADecember 23, 2016device

Brilliance iCT

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

The hazard

During a retrospective review of production documentation it was observed that the M6 Rotor Counterweight Bolt may have been improperly torqued.

What to do

FDA enforcement status: Terminated

Brands named

philips medical systems clevelandphilipsphilips medical

UPCs

453567394382

Recall history

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

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