Product Wiki · Recalls · U.S. FDA — Device Enforcement

Synthes Titanium Cannulated Humeral Nail Intended to aid in the alignment and stabilization of humeral fractures — recall Z-0407-2014

U.S. FDA — Device Enforcement · United States · 2013-07-30 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0407-2014
Date of alert
2013-07-30
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Synthes USA HQ, Inc.
Product category
device
Product type
Devices
Reported risk: The packaging incorrectly depicts the Synthes Titanium Cannulated Humeral Nail as a 3 distal hole nail instead of a 2 distal locking hole nail.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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