NexGen Complete Knee Solution Monoblock Tibial Provisional / Drill… — Class II medical device recall Z-0851-2015
Terminated recall by Zimmer Trabecular Metal Technology, Inc., reported 2014-12-31. During cleaning, two separate units of the NexGen Tibial Base plates did not fit with the Tibial Base Plate ha
| Recall number | Z-0851-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Trabecular Metal Technology, Inc., Parsippany, NJ, United States |
| Recall initiated | 2014-12-02 |
| Classified | 2014-12-23 |
| Reported by FDA | 2014-12-31 |
| Terminated | 2015-08-28 |
| Countries outside the US | AU, DK |
| Quantity | 8 units |
| Lot numbers | 62592928 |
| Model numbers | 00-5887-045-00 |
Product
NexGen Complete Knee Solution Monoblock Tibial Provisional / Drill Guide Tibial Size 5 Femoral Size Green / CH Zimmer U.K. Ltd., SN3 4FP, UK Zimmer Trabecular Metal Technology, Inc 10 Pomeroy Road, Parsippany, NJ 07054 USA
Reason for recall
During cleaning, two separate units of the NexGen Tibial Base plates did not fit with the Tibial Base Plate handle.
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-0851-2015. 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.