Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Affixus Hip Fracture Nail Left 125 9 mm x 300 mm Recalled by Zimmer Biomet, Inc. Due to There were complaints indicating that when the product...
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
Affixus Hip Fracture Nail Left 125 9 mm x 300 mm, Item Number 814409300 Product Usage: Intended for the fixation of fractures
Quantity: 78
Why Was This Recalled?
There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.
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