REF 130-03-738 — Class II medical device recall Z-0626-2024
Completed recall by Encore Medical, LP, reported 2024-01-10, distributed nationwide. Mislabeling
| Recall number | Z-0626-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Encore Medical, LP, Austin, TX, United States |
| Recall initiated | 2023-10-05 |
| Classified | 2024-01-02 |
| Reported by FDA | 2024-01-10 |
| Distributed | Nationwide (US) |
| Quantity | 2 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00888912108560 |
| Lot numbers | 130-03-738, 157N1556 |
| Model numbers | 130-03-738 |
Product
REF 130-03-738, All-Poly e + Patella, Domed Tri-Peg, 9x38mm, STERILE H2O2
Reason for recall
Mislabeling
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-0626-2024. 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.