Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ZMS Intramedullary Fixation Smooth Guide Wire 3.0 mm Diameter Recalled by Zimmer Biomet, Inc. Due to Potential failure of sterile packaging seal.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Zimmer Biomet, Inc. directly.
Affected Products
ZMS Intramedullary Fixation Smooth Guide Wire 3.0 mm Diameter, 100 cm Length; Item Number: 47-2237-037-00
Quantity: 19483 total products
Why Was This Recalled?
Potential failure of sterile packaging seal.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Zimmer Biomet, Inc.
Zimmer Biomet, Inc. has 875 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report