Device recall
Z-0091-2021: Levo Arm Label: LEVO ARM REF 7887-050 MIZUHO OSI Refurbished Levo Arm Label…
FDA device recall · Class II · Mizuho OSI
Key facts
| Recall number (Z-number) | Z-0091-2021 |
|---|---|
| Recall event | 86482 |
| Product | Levo Arm Label: LEVO ARM REF 7887-050 MIZUHO OSI Refurbished Levo Arm Label: LEVO ARM REF 7887-050R MIZUHO OSI - Product Usage: used with Mizuho OSI spinal surgery tables to provide patient head support and positioning during spinal surgery. |
| Product code | JEA |
| Recalling firm | Mizuho OSI |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 27, 2023 |
| FEI number | 2921578 |
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