FDA Device recall Z-0851-2015
NexGen Complete Knee Solution Monoblock Tibial Provisional / Drill Guide Tibial Size 5 Femoral Size Green / CH Zimmer U.K. Ltd., SN3 4FP, U…
- FDA Device
- Class II
- terminated
- Published 2014-12-31
On 2014-12-31 the FDA classified a Class II recall of NexGen Complete Knee Solution Monoblock Tibial Provisional / Drill Guide Tibial Size 5 Femoral Size Green / CH Zimmer U.K. Ltd., SN3 4FP, U… by Zimmer Trabecular Metal Technology, citing during cleaning, two separate units of the NexGen Tibial Base plates did not fit with the Tibial Base Plate handle.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0851-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-12-02 |
| Published | 2014-12-31 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Zimmer Trabecular Metal Technology |
| Distribution | n/a |
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
During cleaning, two separate units of the NexGen Tibial Base plates did not fit with the Tibial Base Plate handle.
Identifiers
| code_info | Part number 00-5887-045-00 Lot number 62592928 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
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All Zimmer Trabecular Metal Technology recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0851-2015%22
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