2M insert 15degree for MUTARS RS cup and LUMiC TiN orthopedic hip… — Class II medical device recall Z-2517-2018
Terminated recall by IMPLANTCAST GMBH, reported 2018-08-01, distributed in GA, RI, TX. Possibility that the retaining ring in the 2M inlay 15degree for MUTARS RS Cup and LUMiC TiN is incorrectly mo
| Recall number | Z-2517-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | IMPLANTCAST GMBH, Buxtehude, N/A, Germany |
| Recall initiated | 2017-12-28 |
| Classified | 2018-07-20 |
| Reported by FDA | 2018-08-01 |
| Terminated | 2020-09-01 |
| Distributed | GA, RI, TX |
| Quantity | 304 |
| Lot numbers | 150201G, 1504298, 1504299, 150429C, 150429L, 15042A5, 15042A6, 15042A7, 15042AF, 16141C1, 16141C2, 1637108, 1637109, 1702188, 1702189 |
| Model numbers | 02423839, 02424244, 02424448, 02424652 |
Product
2M insert 15degree for MUTARS RS cup and LUMiC TiN orthopedic hip implant acetabular component. Size 38/39 mm REF number 02423839 Size 42/44 mm REF number 02424244 Size 44/48 mm REF number 02424448 Size 46/52 mm REF number 02424652
Reason for recall
Possibility that the retaining ring in the 2M inlay 15degree for MUTARS RS Cup and LUMiC TiN is incorrectly mounted.
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-2517-2018. 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.