Home / Recalls / Medical Devices
Synthes USA HQ, Inc. recalls Synthes Cannulated Distal Femoral Nail (Trauma Nail), Part Number 450.851S, 420MM-Sterile. Orthppedic implant device.
Recalled September 25, 2013 · FDA recall Z-2243-2013 · Synthes USA HQ
Hazard
Firm discovered that a nail that was within the scope of a previous Trauma Nail recall had been distributed. · FDA Class II
Units
1
Sold at
US distribution to MA.
Description
Firm discovered that a nail that was within the scope of a previous Trauma Nail recall had been distributed.
Product
Synthes Cannulated Distal Femoral Nail (Trauma Nail), Part Number 450.851S, 420MM-Sterile. Orthppedic implant device.
Manufacturer(s)
Synthes USA HQ, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →