Device recall
Z-0851-2015: NexGen Complete Knee Solution Monoblock Tibial Provisional / Drill Guide Tibial…
FDA device recall · Class II · Zimmer Trabecular Metal Technology, Inc.
Key facts
| Recall number (Z-number) | Z-0851-2015 |
|---|---|
| Recall event | 69866 |
| 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 |
| Product code | HXB |
| Recalling firm | Zimmer Trabecular Metal Technology, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 28, 2015 |
| FEI number | 3005751028 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database