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

The Synthes Hohmann Retractor, 43 mm Long Shank, Angled 235 mm Product Usage: Used to expose bone for procedures. — recall Z-1457-2014

U.S. FDA — Device Enforcement · United States · 2014-02-11 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1457-2014
Date of alert
2014-02-11
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Synthes, Inc.
Product category
device
Product type
Devices
Reported risk: The Synthes Hohmann Retractor was mis-etched on the product and package as part number 399.24 instead of part number 399.22.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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