EVA Floor Lifts — Class II medical device recall Z-1943-2020
Ongoing recall by Handicare AB, reported 2020-05-20. After feedback from customers and internal suspicion, Handicare has become aware that abnormal use of Eva-lift
| Recall number | Z-1943-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Handicare AB, Lulea, N/A, Sweden |
| Recall initiated | 2016-06-15 |
| Classified | 2020-05-08 |
| Reported by FDA | 2020-05-20 |
| Countries outside the US | MX |
| Quantity | 997 units |
| Model numbers | 400, 450, 600 |
Product
EVA Floor Lifts, Model Numbers: 400, 450, 600
Reason for recall
After feedback from customers and internal suspicion, Handicare has become aware that abnormal use of Eva-lifts could lead to a deterioation in the joint of the liftarm. This could lead to injury if the joint breaks. All lifts must therefore be checked and reported back to the manuafacturer.
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-1943-2020. 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.