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FDANovember 10, 2014device

GE Optional Laser Centering Device X-ray generator.

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

The hazard

GE has identified a potential failure to comply with 21 C.F.R. ¿ 1040.10 and 21 C.F.R. ¿ 1010.2 for the alignment laser centering device.

What to do

FDA enforcement status: Terminated

Brands named

ge inspection technologies lp

Recall history

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

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