ATTUNE Revision Tibial Augment Size 7/8 5mm- intended for knee joint… — Class II medical device recall Z-0074-2022
Terminated recall by DePuy Orthopaedics, Inc., reported 2021-10-13, distributed nationwide. Packaging may include screws that are not intended to be used with the 5mm augments, may cause delay in surger
| Recall number | Z-0074-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | DePuy Orthopaedics, Inc., Warsaw, IN, United States |
| Recall initiated | 2021-09-09 |
| Classified | 2021-10-07 |
| Reported by FDA | 2021-10-13 |
| Terminated | 2023-08-09 |
| Distributed | Nationwide (US) |
| Quantity | 10 units |
| UPC / GTIN / UDI-DI | 10603295057642 |
| Lot numbers | J6304Z |
| Model numbers | 152307001 |
Product
ATTUNE Revision Tibial Augment Size 7/8 5mm- intended for knee joint replacement Part Code:152307001
Reason for recall
Packaging may include screws that are not intended to be used with the 5mm augments, may cause delay in surgery
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-0074-2022. 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.