Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
TRABECULAR METAL MODULAR ACETABULAR SYSTEM Recalled by Zimmer, Inc. Due to The shell was missing the locking ring.
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, Inc. directly.
Affected Products
TRABECULAR METAL MODULAR ACETABULAR SYSTEM, Shell with Cluster Holes, Porous 60mm. Catalog number 00-6202-060-22; Hip implant component.
Quantity: 17 units
Why Was This Recalled?
The shell was missing the locking ring.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Zimmer, Inc.
Zimmer, Inc. has 437 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report