COR Disposable Kit — Class II medical device recall Z-1315-2025
Ongoing recall by DePuy Mitek, Inc., a Johnson & Johnson Co., reported 2025-03-19, distributed nationwide. Device is missing the pin in the graft loader component.
| Recall number | Z-1315-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | DePuy Mitek, Inc., a Johnson & Johnson Co., Norwood, MA, United States |
| Recall initiated | 2025-02-24 |
| Classified | 2025-03-11 |
| Reported by FDA | 2025-03-19 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, BE, BR, CH, CL, CN, CO, CZ, DE, ES, FI, FR, GR, GY, IL, IN, IT, JP, KR, MX, NL, PL, PT, SG |
| UPC / GTIN / UDI-DI | 10886705012374, 10886705012404 |
| Lot numbers | 23C11, 23C12, 23C13, 23D03, 23D14, 23E04, 23F01, 23F02, 23R03, 24A02, 24B01, 24C15, 24C17, 24K07, 24N10, 24P07 |
| Model numbers | 252109, 252112 |
Product
COR Disposable Kit, 8 mm w/ Perpendicularity. Cartilage Transplant System.
Reason for recall
Device is missing the pin in the graft loader component.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1315-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.