Device recall
Z-0953-03: Allen Medical Systems PAL Pro Stirrups Catalog Number: A-10051-A1
FDA device recall · Class II · The OR Group,Inc.
Key facts
| Recall number (Z-number) | Z-0953-03 |
|---|---|
| Recall event | 26439 |
| Product | Allen Medical Systems PAL Pro Stirrups Catalog Number: A-10051-A1 |
| Product code | FWZ |
| Recalling firm | The OR Group,Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 2, 2016 |
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