Class II — Altimate Medical, Inc.
| Recalling firm | Altimate Medical, Inc. |
|---|---|
| Registered facility | ALTIMATE MEDICAL, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| 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. |
| Product | ActiveAid 922, Shower/Commode Chair |
| Quantity | 1 unit |
| Distribution | US Nationwide distribution in the state of Texas. |
| Initiated | 2022-11-30 |
| Classified | 2023-01-04 |
| Terminated | 2023-08-31 |
| Recall number | Z-0880-2023 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Altimate Medical, Inc. (Z-0880-2023).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/91335/
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