DePuy Mitek recalls COR Disposable Kit 8mm with Perpendicularity for cartilage transplant. Missing pin in graft loader component may cause improper implant placement.
Device is missing the pin in the graft loader component.
DePuy Mitek is recalling COR Disposable Kit 8mm cartilage transplant systems because the graft loader component may be missing the pin. This could lead to improper implant placement during surgery.
The graft loader component may be missing the pin, which is critical for proper implant placement during cartilage transplant surgery. This could result in improper positioning of the implant.
Surgical patients and medical professionals using DePuy Mitek COR Disposable Kit 8mm cartilage transplant systems. The risk is low as the hazard is specific to the graft loader component.
Check for model numbers 252109 or 252112, GTINs 10886705012374 or 10886705012404, or lot numbers listed in the recall notice.
Verify the model number is 252109 or 252112 to confirm if the product is affected.
Reach out to DePuy Mitek for specific guidance on the recall if you have the product.
The recall indicates the graft loader component may be missing the pin, which could lead to improper implant placement. Do not use if you have the affected model numbers.
Check the model number and lot number to confirm if you have the recalled product. Contact DePuy Mitek for further instructions.
Affected products have model numbers 252109 or 252112, GTINs 10886705012374 or 10886705012404, or specific lot numbers listed in the recall notice.
We’ve drafted a message you can send DePuy Mitek to request your refund or repair — edit it as you like.
Subject: Recall Z-1315-2025 — DePuy Mitek DePuy Mitek Hello, I own a DePuy Mitek that is covered by recall Z-1315-2025 from DePuy Mitek. 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.