Device recall
Z-1362-2008: Biomet Vanguard Knee Instrumentation, Part Number: 32-487062, 67.5/70/75mm…
FDA device recall · Class II · Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-1362-2008 |
|---|---|
| Recall event | 46706 |
| Product | Biomet Vanguard Knee Instrumentation, Part Number: 32-487062, 67.5/70/75mm Sizing Wing, Biomet UK Ltd, Made in Britain; The device is a preparatory instrument used for femoral knee insertion. (Distributed to Puerto Rico). |
| Product code | HWT |
| Recalling firm | Biomet, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 26, 2009 |
| FEI number | 1825034 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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