NexGen LCCK Legacy Articular Surface with Locking Screw — Class II medical device recall Z-1039-2025
Ongoing recall by Zimmer, Inc., reported 2025-02-05, distributed nationwide. It was identified internally that two commingle events occurred where the metal support post within the polyet
| Recall number | Z-1039-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer, Inc., Warsaw, IN, United States |
| Recall initiated | 2025-01-06 |
| Classified | 2025-01-28 |
| Reported by FDA | 2025-02-05 |
| Distributed | Nationwide (US) |
| Countries outside the US | CN, IN, KR, MY, NL, SG, TW |
| Quantity | 155 units |
| UPC / GTIN / UDI-DI | 00889024635746 |
| Lot numbers | 66782840, 66782843, 66873137 |
| Model numbers | 00-5994-032-10 |
Product
NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Yellow/E,F - Height 10 mm, Item Number 00-5994-032-10
Reason for recall
It was identified internally that two commingle events occurred where the metal support post within the polyethylene articular surface was assembled incorrectly for three units within the scope.
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-1039-2025. 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.