Device recall
Z-0880-2023: ActiveAid 922, Shower/Commode Chair
FDA device recall · Class II · Altimate Medical, Inc.
Key facts
| Recall number (Z-number) | Z-0880-2023 |
|---|---|
| Recall event | 91335 |
| Product | ActiveAid 922, Shower/Commode Chair |
| Product code | INN |
| Recalling firm | Altimate Medical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 31, 2023 |
| FEI number | 2183634 |
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