Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
NexGen TRABECULAR METAL FEMORAL AUGMENT BLOCK DISTAL ONLY Recalled by Zimmer Trabecular Metal Technology, Inc. Due to Mislabeling
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 Trabecular Metal Technology, Inc. directly.
Affected Products
NexGen TRABECULAR METAL FEMORAL AUGMENT BLOCK DISTAL ONLY, 20 MM Augment, Size D, Sterile, Rx Only. Product Usage: Intended for use where severe degeneration, trauma, or other pathology of the knee joint indicates total knee arthroplasty. When used with the NexGen Complete Knee Solution-Rotating Hinge Knee (RHK) System, the Trabecular Metal Augments are for cemented use only. When used with the NexGen Complete Knee Solution-Legacy Constrained Condylar Knee System, the Trabecular Metal Augments are for cementless or cemented use.
Quantity: 1 unit
Why Was This Recalled?
One unit of the 20 mm augments was mislabeled as 5 mm and it was subsequently distributed.
Where Was This Sold?
This product was distributed to 1 state: CA
About Zimmer Trabecular Metal Technology, Inc.
Zimmer Trabecular Metal Technology, Inc. has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report