NexGen Precoat Stemmed Tibial Plate Size 5 — Class II medical device recall Z-2092-2023
Terminated recall by Zimmer, Inc., reported 2023-07-12. Device outer packaging was incorrectly labeled.
| Recall number | Z-2092-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer, Inc., Warsaw, IN, United States |
| Recall initiated | 2023-05-19 |
| Classified | 2023-07-05 |
| Reported by FDA | 2023-07-12 |
| Terminated | 2026-05-29 |
| Countries outside the US | IN |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00889024217607 |
| Model numbers | 00598004701 |
Product
NexGen Precoat Stemmed Tibial Plate Size 5
Reason for recall
Device outer packaging was incorrectly labeled.
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-2092-2023. 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.