ATTUNE Revision CRS Femoral LT SZ 5 Cemented — Class II medical device recall Z-1703-2018
Terminated recall by DePuy Orthopaedics, Inc., reported 2018-05-16, distributed in FL, MO, PA. There may be burrs on the extraction hole threads.
| Recall number | Z-1703-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | DePuy Orthopaedics, Inc., Warsaw, IN, United States |
| Recall initiated | 2018-04-16 |
| Classified | 2018-05-07 |
| Reported by FDA | 2018-05-16 |
| Terminated | 2019-04-02 |
| Distributed | FL, MO, PA |
| Quantity | 2 units |
| UPC / GTIN / UDI-DI | 10603295042181 |
| Lot numbers | HC1179, HC1183 |
| Model numbers | 150440105 |
Product
ATTUNE Revision CRS Femoral LT SZ 5 Cemented, Catalog No. 150440105, Femoral Revision Implant, Knee
Reason for recall
There may be burrs on the extraction hole threads.
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-1703-2018. 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.