FDA Device recall Z-1943-2020
EVA Floor Lifts, Model Numbers: 400, 450, 600
- FDA Device
- Class II
- ongoing
- Published 2020-05-20
On 2020-05-20 the FDA classified a Class II recall of EVA Floor Lifts, Model Numbers: 400, 450, 600 by Handicare Ab, citing 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 coul….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1943-2020 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2016-06-15 |
| Published | 2020-05-20 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Handicare Ab |
| Distribution | n/a |
Product
EVA Floor Lifts, Model Numbers: 400, 450, 600
Reason
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.
Identifiers
| code_info | All affected models |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1943-2020%22
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