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MicroAire Surgical Instruments, LLC recalls Endotine Transbleph 3.5 (CFD-080-0167)
Recalled August 3, 2016 · FDA recall Z-2294-2016 · MicroAire Surgical Instruments
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). · FDA Class II
Units
29
Sold at
The product was distributed in the United States and Sweden
Description
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).
Product
Endotine Transbleph 3.5 (CFD-080-0167)
Manufacturer(s)
MicroAire Surgical Instruments, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →