FDAMay 6, 2016device

Endotine Transbleph 3.5 (CFD-080-0167)

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

The hazard

MicroAire has initiated a limited recall (29 Units)on the Endotine Transbleph 3.5 (CFD-080-0167), Lot # 285373, due to minor mislabeling ( the front label is correct, but the side label lists an incorrect part number, i.e. CFD-080-0177).

What to do

FDA enforcement status: Terminated

Brands named

microaire surgical instrumentsmicroairemicroaire surgical

Recall history

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

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