# FDA recall Z-1943-2020

> **Handicare AB** · Class II · device recall initiated 2016-06-15.

## 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.

## Distribution

US and Mexico

## Key facts

- **Recall number:** Z-1943-2020
- **Recalling firm:** Handicare AB
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2016-06-15
- **Report date:** 2020-05-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lulea, N/A, Sweden

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1943-2020

## Citation

> AI Analytics. FDA recall Z-1943-2020. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-1943-2020. Source: US FDA. Licensed CC0.

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