Home / Recalls / Medical Devices
Synthes USA HQ, Inc. recalls Synthes Trauma Nail System. The devices are indication for bone fixation.
Recalled September 4, 2013 · FDA recall Z-2058-2013 · Synthes USA HQ
Hazard
Recall was initiated due to the possibility that the outer pouch was compromised. The product is packaged in two pouches; a sterile, internal pouch within an external pouch. It is the outer, external pouch that may be compromised. · FDA Class II
Units
1,011,783
Sold at
Nationwide distribution.
Description
Recall was initiated due to the possibility that the outer pouch was compromised. The product is packaged in two pouches; a sterile, internal pouch within an external pouch. It is the outer, external pouch that may be compromised.
Product
Synthes Trauma Nail System. The devices are indication for bone fixation.
Manufacturer(s)
Synthes USA HQ, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →