Home / Recalls / Medical Devices
Zimmer Biomet, Inc. recalls M/DN Intramedullary Fixation Humeral Guide Wire - Smooth 2.4 mm Diameter 70 cm Length Single Use Only; Item Number: 00-2
Recalled May 2, 2018 · FDA recall Z-1465-2018 · Zimmer Biomet
Hazard
Potential failure of sterile packaging seal. · FDA Class II
Units
19483 total products
Sold at
US Nationwide and the following countries: Brazil, Singapore, Canada, Australia, Japan, Malaysia, Chile, Netherlands, Trinidad
Description
Potential failure of sterile packaging seal.
Product
M/DN Intramedullary Fixation Humeral Guide Wire - Smooth 2.4 mm Diameter 70 cm Length Single Use Only; Item Number: 00-2255-025-00
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →