Zimmer Biomet recalls NCB-PH plates made before January 2014 due to risk of implants sticking to LDPE packaging during use.
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
Zimmer Biomet is recalling certain NCB-PH plates made before January 2014 because non-highly polished implants might stick to the plastic packaging. This could cause issues during surgery if the implant becomes stuck.
Non-highly polished implants can adhere to the LDPE (plastic) packaging. This might cause the implant to become stuck during surgery, potentially requiring additional procedures.
Orthopedic surgeons and medical facilities using the recalled plates. Patients undergoing hip or knee surgery are most at risk if the implant sticks during procedure.
Check for item numbers 0202262104, 0202262105, or 0202262107 on the plate. Products made before January 2014 are affected.
Look for item numbers 0202262104, 0202262105, or 0202262107 on the plate.
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
The recall does not specify a remedy, so contact Zimmer Biomet directly for guidance.
The hazard involves potential implant sticking during surgery, but the recall indicates low risk.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-0332-2020 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-0332-2020 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.
