ActiveAid 922 — Class II medical device recall Z-0880-2023
Terminated recall by Altimate Medical, Inc., reported 2023-01-11, distributed nationwide. Device manufactured with a component with affects the foldability of the frame, not allowing it to be secured
| Recall number | Z-0880-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Altimate Medical, Inc., Morton, MN, United States |
| Recall initiated | 2022-11-30 |
| Classified | 2023-01-04 |
| Reported by FDA | 2023-01-11 |
| Terminated | 2023-08-31 |
| Distributed | Nationwide (US) |
| Quantity | 1 units |
| Serial numbers | 90071504001 |
Product
ActiveAid 922, Shower/Commode Chair
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0880-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.