Reported Mar 19, 2025 · Ongoing
COR Disposable Kit, 8 mm. Cartilage Transplant System.
DePuy Mitek, Inc., a Johnson & Johnson Co.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: DePuy Mitek, Inc., a Johnson & Johnson Co. · 249 Vanderbilt Ave · Norwood, MA · 02062-5033
Is this the product you have?
- COR Disposable Kit, 8 mm. Cartilage Transplant System.
- Lot codes and dates
- Model No. 252109 & 252112
- GTIN
10886705012374 & 10886705012404Lot No. 23C1123C1223E0423F0223R0324A0224B0124C1724P0723C1323D0323D1423F0124C1524K07 & 24N10
- Amount recalled
- US: 131 units; OUS: 312 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
Why it was recalled
Device is missing the pin in the graft loader component.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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