Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DELTA CER FEM HD 32/0MM T1 Product Usage: For use in hip arthroplasty Recalled by Zimmer Biomet, Inc. Due to Product may contain the presence of melted sterile...
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
DELTA CER FEM HD 32/0MM T1 Product Usage: For use in hip arthroplasty
Quantity: 30
Why Was This Recalled?
Product may contain the presence of melted sterile packaging upon opening.
Where Was This Sold?
US in the state of Texas
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