Device recall
Z-1223-2012: Vanguard Knee Instrumentation Tibial Resection Tower Universal with alignment…
FDA device recall · Class II · Biomet U.K., Ltd.
Key facts
| Recall number (Z-number) | Z-1223-2012 |
|---|---|
| Recall event | 61274 |
| Product | Vanguard Knee Instrumentation Tibial Resection Tower Universal with alignment tower geometry, REF 32487557, LOT 2561334, Biomet UK Ltd, South Wales, UK Product Usage: Usage: Used to guide a saw blade in resecting the proximal tibia. Intended to be used with a tibial alignment guide. |
| Product code | LXH |
| Recalling firm | Biomet U.K., Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 6, 2012 |
| FEI number | 3002806535 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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