A-series lift — Class II medical device recall Z-1405-2017
Terminated recall by ErgoSafe Products, LLC (DBA) Prism Medical, reported 2017-03-15, distributed in MT, NV. During internal cycle test at max load (625 lbs.) 2 units had straps break prematurely.
| Recall number | Z-1405-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | ErgoSafe Products, LLC (DBA) Prism Medical, Maryland Heights, MO, United States |
| Recall initiated | 2017-01-30 |
| Classified | 2017-03-03 |
| Reported by FDA | 2017-03-15 |
| Terminated | 2017-12-04 |
| Distributed | MT, NV |
| Quantity | 21 |
| Reason classes | device malfunction |
| Model numbers | 324124 |
Product
A-series lift - A625 Manual w/Load Cell & Wi-Fi, Omni Part No. 324124. Prism Medical.
Reason for recall
During internal cycle test at max load (625 lbs.) 2 units had straps break prematurely.
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-1405-2017. 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.