Zimmer recalls specific NexGen LCCK Legacy Articular Surface models due to potential incorrect assembly of the metal support post, which could affect joint stability.
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 with a locking screw. The recall is because three units were found to have the metal support post assembled incorrectly, which could lead to joint instability.
The metal support post inside the polyethylene articular surface was assembled incorrectly in three units. This could cause joint instability if the implant is used as intended.
Patients who received the recalled NexGen LCCK Legacy Articular Surface implants with the specific model and item number are affected. Those with joint replacements using this model are most at risk.
Check for the NexGen LCCK Legacy Articular Surface with Locking Screw, striped yellow/E,F, height 10 mm, item number 00-5994-032-10. Lot numbers 66782843, 66782840, and 66873137 are also associated with this recall.
Verify the item number, lot numbers, and model specifications to confirm if your implant is part of this recall.
Zimmer identified that three units had the metal support post assembled incorrectly, which could affect joint stability.
Check for the specific model: NexGen LCCK Legacy Articular Surface with Locking Screw, striped yellow/E,F, height 10 mm, item number 00-5994-032-10, and lot numbers 66782843, 66782840, or 66873137.
The recall does not specify a remedy, so contact Zimmer directly for guidance on next steps.
We’ve drafted a message you can send Zimmer to request your refund or repair — edit it as you like.
Subject: Recall Z-1039-2025 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-1039-2025 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.
