Zimmer Biomet recalls 14MM Intramedullary Bone Saw Cam Assemblies with possible 13MM size mismatch. Affected units have specific lot numbers and UDI codes. Contact for return or replacement.
Possible commingle of 13 MM and 14 MM Intramedullary Bone Saw Cam Assembly -an Intramedullary Bone Saw Cam Assembly was labeled and etched as a 14 MM but measured as a 13 MM cam
Zimmer Biomet is recalling certain 14MM Intramedullary Bone Saw Cam Assemblies due to a possible size mismatch. The product may be labeled as 14MM but measure 13MM, which could lead to improper surgical use.
The cam assembly is labeled as 14MM but may measure 13MM. This size discrepancy could lead to improper surgical application if the wrong size is used during procedures.
Orthopedic surgeons and medical professionals who use the recalled bone saw cam assemblies. The risk is low as this is a size mismatch issue in surgical instruments.
Check for lot numbers 334360, 366680, or 366670 on the product. The unique device identifier (UDI) codes include specific sequences for these lots.
Review the lot numbers and UDI codes on the product to confirm if it is affected.
The cam assembly is labeled as 14MM but may measure 13MM, which could lead to improper surgical use.
Lot numbers 334360, 366680, and 366670.
Check the product for lot numbers 334360, 366680, or 366670 and verify the UDI codes.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-0595-2020 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-0595-2020 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.
