Device recall
Z-0702-2008: Biomet RINGLOC + Instrumentation Impactor Plate, Size 22; REF/Part#: 31-400622…
FDA device recall · Class II · Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-0702-2008 |
|---|---|
| Recall event | 45987 |
| Product | Biomet RINGLOC + Instrumentation Impactor Plate, Size 22; REF/Part#: 31-400622, Biomet Orthopedics, Inc., Warsaw, IN. |
| Product code | LXH |
| Recalling firm | Biomet, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 11, 2008 |
| FEI number | 1825034 |
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