Device recall
Z-0925-2013: REF S313152 Straight Acetabular Inserter Handle Ringloc non-sterile Orthopedic…
FDA device recall · Class II · Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-0925-2013 |
|---|---|
| Recall event | 64354 |
| Product | REF S313152 Straight Acetabular Inserter Handle Ringloc non-sterile Orthopedic manual surgical instrument |
| Product code | LXH |
| Recalling firm | Biomet, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 30, 2013 |
| 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