Zimmer recalls specific NexGenTrabecular Metal Tibial Half Block Augments due to potential mismatch between product in box and label. Affected items have unique lot numbers and UDI codes. Consumers should verify their product details to avoid incorrect usage.
Potentially comingled, resulting in the product in the box potentially not matching the product on the label
Zimmer is recalling certain NexGenTrabecular Metal Tibial Half Block Augments because the product inside the box might not match what's on the label. This mismatch could lead to improper use during knee surgery, which is serious for patients.
The hazard involves the product in the box potentially not matching the product on the label. This mismatch could cause incorrect surgical application, which may lead to improper knee joint replacement outcomes.
Patients who received the recalled NexGenTrabecular Metal Tibial Half Block Augments for knee surgery are most at risk. The recall affects specific lot numbers and UDI codes used in the U.S. healthcare system.
Check the product label for the lot numbers: 63253751, 63257915, or 63291542. Also, verify the Unique Device Identifier (UDI) codes listed in the recall notice.
Look for the lot numbers 63253751, 63257915, or 63291542 on the product label.
The product in the box may not match the product on the label, which could lead to incorrect surgical application during knee replacement procedures.
Check the product label for the lot numbers 63253751, 63257915, or 63291542. If you have these, contact Zimmer for further instructions.
The recall is for potential mismatch between product in box and label, which could lead to incorrect surgical application. However, the hazard does not describe a risk of serious injury in normal use.
We’ve drafted a message you can send Zimmer to request your refund or repair — edit it as you like.
Subject: Recall Z-1005-2019 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-1005-2019 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.
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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.
