Drug recall
EVA Floor Lifts, Model Numbers: 400, 450, 600
FDA recall event 85362 · Class II · Handicare AB
Key facts
| Event ID | 85362 |
|---|---|
| Recall numbers | Z-1943-2020 |
| Recalling firm | Handicare AB |
| Product type | Devices |
| Products | EVA Floor Lifts, Model Numbers: 400, 450, 600 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| 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… |
| Initiation date | Jun 15, 2016 |
| Report date | May 20, 2020 |
| City | Lulea |
| Country | Sweden |
| FEI number | 3009481053 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: