Zimmer recalls specific NexGen LCCK Legacy Articular Surface units with incorrect metal support assembly. Affected units may have safety issues during use. Contact Zimmer for details.
It was identified internally that two commingle events occurred where the metal support post within the polyethylene articular surface was assembled incorrectly for three units within the scope.
Zimmer is recalling certain NexGen LCCK Legacy Articular Surface implants due to a manufacturing error that could lead to improper assembly of the metal support post. This risk might affect the device's safety during use.
The metal support post inside the polyethylene articular surface was assembled incorrectly for three units. This could potentially lead to improper function or safety issues during use, though the risk is limited to the specific affected units.
Patients who received the specific NexGen LCCK Legacy Articular Surface with Locking Screw (Striped Purple/C,D, Height 14 mm) from Zimmer, Inc. are most at risk. The recall affects a small number of units with incorrect assembly.
Check for the product name 'NexGen LCCK Legacy Articular Surface with Locking Screw', color (Striped Purple/C,D), height (14 mm), and item number 00-5 994-022-14. Also look for lot numbers: 66602503, 66520665, 66881918, or 66949906.
Verify the product name, color, height, and item number to confirm if your unit is affected.
Zimmer identified that two commingle events occurred where the metal support post within the polyethylene articular surface was assembled incorrectly for three units.
Check for the product name 'NexGen LCCK Legacy Articular Surface with Locking Screw', color (Striped Purple/C,D), height (14 mm), item number 00-5994-022-14, and lot numbers: 66602503, 66520665, 66881918, or 66949906.
The recall does not specify a remedy, so contact Zimmer directly for guidance.
We’ve drafted a message you can send Zimmer to request your refund or repair — edit it as you like.
Subject: Recall Z-1038-2025 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-1038-2025 from Zimmer. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
