FDA Device recall Z-0880-2023
ActiveAid 922, Shower/Commode Chair
- FDA Device
- Class II
- terminated
- Published 2023-01-11
On 2023-01-11 the FDA classified a Class II recall of ActiveAid 922, Shower/Commode Chair by Altimate Medical, citing device manufactured with a component with affects the foldability of the frame, not allowing it to be secured by the frame strap in the folded position.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0880-2023 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-11-30 |
| Published | 2023-01-11 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Altimate Medical |
| Distribution | US |
Product
ActiveAid 922, Shower/Commode Chair
Reason
Device manufactured with a component with affects the foldability of the frame, not allowing it to be secured by the frame strap in the folded position.
Identifiers
| code_info | Serial Number 90071504001 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0880-2023%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.