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Synthes (USA) Products LLC recalls Synthes Flexible Shaft, Orthopedic manual surgical instrument The Flexible shafts are intended for use as an optional

Recalled November 30, 2016 · FDA recall Z-0656-2017 · Synthes (USA) Products

Hazard
Non-conforming material used. · FDA Class II
Units
198 units
Sold at
US Nationwide Distribution.

Description

Non-conforming material used.

Product
Synthes Flexible Shaft, Orthopedic manual surgical instrument The Flexible shafts are intended for use as an optional reaming step in intramedullary nailing systems.
Manufacturer(s)
Synthes (USA) Products LLC

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Synthes (USA) Products LLC recalls Synthes Flexible Shaft, Orthopedic manual surgical instrument The Flexible shafts are intended for use as an optional | RecallWatchUSA