ATTUNE AFFIXIUM Cementless Fixed Bearing Knee with 3DP Technology — Class II medical device recall Z-1456-2024
Ongoing recall by DePuy Orthopaedics, Inc., reported 2024-04-10, distributed nationwide. Product incorrectly labelled.
| Recall number | Z-1456-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | DePuy Orthopaedics, Inc., Warsaw, IN, United States |
| Recall initiated | 2024-03-12 |
| Classified | 2024-03-29 |
| Reported by FDA | 2024-04-10 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 5 units |
| UPC / GTIN / UDI-DI | 10603295507451 |
| Lot numbers | JA06A0252 |
| Model numbers | 150621006 |
Product
ATTUNE AFFIXIUM Cementless Fixed Bearing Knee with 3DP Technology, Size 6. Component of the ATTUNE Total Knee Replacement System.
Reason for recall
Product incorrectly labelled.
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-1456-2024. 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.