DePuy Mitek recalls 8mm cartilage transplant kits with missing pin in graft loader component. This could cause improper graft placement during surgery. Affected kits have specific model numbers and lot numbers listed in the recall.
Device is missing the pin in the graft loader component.
DePuy Mitek is recalling 8mm cartilage transplant systems that may have a missing pin in the graft loader component. This could lead to improper graft placement during surgery, potentially causing complications for patients.
The graft loader component may be missing a critical pin, which is necessary for proper alignment of the cartilage graft during surgery. Without this pin, the graft might not be positioned correctly, leading to surgical complications.
Surgical teams using the COR Disposable Kit 8mm Cartilage Transplant System for joint repairs are most at risk. Patients undergoing cartilage transplant procedures with the affected kits could experience complications.
Check for model numbers 252109 or 252112 on the kit packaging. The lot numbers listed include 23C11 through 24N10. These kits were sold with specific GTINs and lot numbers.
Verify the model number on the kit packaging; affected kits have model numbers 252109 or 252112.
Reach out to DePuy Mitek directly for further assistance with the recall.
The graft loader component may be missing a pin, which is necessary for proper alignment of the cartilage graft during surgery.
Check for model numbers 252109 or 252112 on the packaging and lot numbers listed in the recall (23C11 through 24N10).
Contact DePuy Mitek directly for further assistance with the recall.
We’ve drafted a message you can send DePuy Mitek to request your refund or repair — edit it as you like.
Subject: Recall Z-1314-2025 — DePuy Mitek DePuy Mitek Hello, I own a DePuy Mitek that is covered by recall Z-1314-2025 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.
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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.
