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Synthes USA HQ, Inc. recalls Titanium Trochanteric Fixation Nail (TFN)System Intended to treat stable and unstable fractures of the proximal femur
Recalled December 11, 2013 · FDA recall Z-0452-2014 · Synthes USA HQ
Hazard
Two lots of Titanium Trochanteric Fixation Nail (TFN) System are missing the second bend in the nail. · FDA Class II
Units
17
Sold at
Nationwide Distribution including IL, CA, AZ, FL, TX, UT, VA, NY, NM, and MT.
Description
Two lots of Titanium Trochanteric Fixation Nail (TFN) System are missing the second bend in the nail.
Product
Titanium Trochanteric Fixation Nail (TFN)System Intended to treat stable and unstable fractures of the proximal femur.
Manufacturer(s)
Synthes USA HQ, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →