Zimmer recalls specific NexGen Tibial Half Block Augments due to potential mismatch between product in box and label. Affected items have unique lot numbers; consumers should verify their product details.
Potentially comingled, resulting in the product in the box potentially not matching the product on the label
Zimmer is recalling certain NexGen Tibial Half Block Augments because the product inside the box might not match what's on the label. This mismatch could lead to incorrect use in knee surgery, which is serious for patients.
The product in the box may not match the label, which could mean the wrong size or type of implant is used during knee surgery. This mismatch could lead to incorrect surgical outcomes if the implant doesn't fit properly.
Patients who received the recalled NexGen Tibial Half Block Augments for knee surgery are most at risk. The recall affects specific lot numbers used in certain surgical procedures.
Check the product label for the lot numbers: 63244259, 63247617, 63279968, 61581585T, or 00889024307902 (17) with specific date codes. These items were sold for knee surgery procedures.
Look for lot numbers on the product label: 63244259, 63247617, 63279968, 61581585T, or 00889024307902 (17) with specific date codes.
The product in the box may not match the label, which could lead to incorrect use during knee surgery.
Check the product label for the specific lot numbers listed in the recall notice. If you have the recalled items, you should verify with your surgeon.
The recall is due to a potential mismatch between the product in the box and the label, which could lead to incorrect surgical outcomes if the implant doesn't fit properly.
We’ve drafted a message you can send Zimmer to request your refund or repair — edit it as you like.
Subject: Recall Z-1006-2019 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-1006-2019 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
