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Zimmer Biomet, Inc. recalls ZMS Intramedullary Fixation Smooth Guide Wire 3.0 mm Diameter, 100 cm Length; Item Number: 47-2237-037-00
Recalled May 2, 2018 · FDA recall Z-1470-2018 · 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
ZMS Intramedullary Fixation Smooth Guide Wire 3.0 mm Diameter, 100 cm Length; Item Number: 47-2237-037-00
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →