Molift Smart 150 — Class II medical device recall Z-1343-2013
Terminated recall by Moller Vital, reported 2013-05-29, distributed nationwide. The leg spreading mechanism will fail to hoist and collapse if assemble incorrectly by the user.
| Recall number | Z-1343-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Moller Vital, Gjovik, N/A, Norway |
| Recall initiated | 2013-02-15 |
| Classified | 2013-05-21 |
| Reported by FDA | 2013-05-29 |
| Terminated | 2014-07-11 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, BE, CH, DE, DK, ES, FI, FR, GB, IL, IS, IT, JP, NL, NO, NZ |
Product
Molift Smart 150
Reason for recall
The leg spreading mechanism will fail to hoist and collapse if assemble incorrectly by the user.
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-1343-2013. 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.