Device recall
Z-0802-2019: ARJOHUNTLEIGH GETINGE GROUP, RotoProne Therapy System, Model Number 209800
FDA device recall · Class II · Arjohuntleigh Magog
Key facts
| Recall number (Z-number) | Z-0802-2019 |
|---|---|
| Recall event | 81872 |
| Product | ARJOHUNTLEIGH GETINGE GROUP, RotoProne Therapy System, Model Number 209800 |
| Product code | IKZ |
| Recalling firm | Arjohuntleigh Magog |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 26, 2022 |
| FEI number | 3002655016 |
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