EasyStand Bantam — Class II medical device recall Z-0243-2023
Terminated recall by Altimate Medical, Inc., reported 2022-11-23, distributed in CA, CT, FL, LA, MI, TN, TX. Some EasyStand Bantam Small and Extra Small standers with the non-supine option may have been manufactured wit
| Recall number | Z-0243-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Altimate Medical, Inc., Morton, MN, United States |
| Recall initiated | 2022-10-04 |
| Classified | 2022-11-16 |
| Reported by FDA | 2022-11-23 |
| Terminated | 2023-08-31 |
| Distributed | CA, CT, FL, LA, MI, TN, TX |
| Countries outside the US | CA |
| Quantity | 14 devices |
| UPC / GTIN / UDI-DI | 10858921006062, 10858921006079 |
Product
EasyStand Bantam, with the following sizes. a. Small; b. Extra Small. Used for assisting individual in standing.
Reason for recall
Some EasyStand Bantam Small and Extra Small standers with the non-supine option may have been manufactured with a component that affects the operation of the leg assembly bracket to maintain the standers non-supine 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-0243-2023. 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.