Zimmer Biomet recalls NCB Straight Narrow Plate implants made before January 2014 due to potential adhesion to LDPE packaging. Affected items may require replacement to prevent complications.
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
Zimmer Biomet is recalling NCB Straight Narrow Plate implants produced before January 2014. These implants could stick to their original LDPE packaging, potentially causing issues during surgery.
The implants may adhere to the LDPE packaging during handling or storage. This could lead to the implant becoming stuck in the packaging, potentially causing complications during surgical procedures.
Orthopedic surgeons and patients who have received the recalled implants made before January 2014. Those using the implants in surgical procedures are most at risk.
Check for the product model numbers 0202267008, 0202267010, 0202267012, 0202267014, 0202267016, or 0202267018. The implants were manufactured before January 2014.
Identify the model number on the implant to see if it matches the recalled numbers.
Reach out to Zimmer Biomet for guidance on next steps if the implant is recalled.
The recall indicates a potential risk of adhesion to packaging, but the implants are generally safe. Affected users should contact Zimmer Biomet for specific advice.
If you have the recalled model numbers made before January 2014, contact Zimmer Biomet for instructions on replacement or further action.
The recall record does not specify a fix; users should contact Zimmer Biomet directly for guidance.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-0331-2020 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-0331-2020 from Zimmer Biomet. 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.
