Device recall
Z-2230-2009: Maxi Move Scoop Stretcher; Note: The stretcher is an accessory to the Maxi Move…
FDA device recall · Class II · ArjoHuntleigh
Key facts
| Recall number (Z-number) | Z-2230-2009 |
|---|---|
| Recall event | 52824 |
| Product | Maxi Move Scoop Stretcher; Note: The stretcher is an accessory to the Maxi Move Patient Lift; Made by Arjo Hospital Equipment AB, Eslov, Sweden; product number KRA2210-20. |
| Product code | FSA |
| Recalling firm | ArjoHuntleigh |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 7, 2010 |
| FEI number | 3007515958 |
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