Device recall
Z-1480-2009: Biomet Optivac Total Hip Kit, Maximum Capacity Cartridge, 1 kit, sterile, latex…
FDA device recall · Class III · Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-1480-2009 |
|---|---|
| Recall event | 52009 |
| Product | Biomet Optivac Total Hip Kit, Maximum Capacity Cartridge, 1 kit, sterile, latex free, Biomet Orthopedics, Inc., Warsaw, IN; Product Number: 418000. Vacuum mixing and vacuum collection system and application system for bone cement. |
| Product code | JDZ |
| Recalling firm | Biomet, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Oct 6, 2010 |
| 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