Device recall
Z-2229-2010: SpeedPass Disposable Suture Lariat with Nitinol Wire 25 Degree Left, QTY. 1…
FDA device recall · Class II · Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-2229-2010 |
|---|---|
| Recall event | 56193 |
| Product | SpeedPass Disposable Suture Lariat with Nitinol Wire 25 Degree Left, QTY. 1, Biomet Sports Medicine, Warsaw, IN 46581. Sterile. Part number 904010. Used to pass suture through tissue. |
| Product code | MDM |
| Recalling firm | Biomet, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 6, 2012 |
| 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