# FDA recall Z-1352-2019

> **Moller Vital** · Class II · device recall initiated 2019-02-04.

## Product

Molift 2-Point sling bar, an accessory for Molift Mover 180/Air. Item nos. 1830001  1830002  1830002C  1830003

## Reason for recall

The firm has received 7 reports of malfunction for the device in which the hooks have broken off, potentially leading the sling to slip out of the sling bar and causing the patient to fall.

## Distribution

Domestic distribution to Arizona, Delaware, Florida, Georgia, Massachusetts, Ohio, South Carolina, Texas, Washington, and Wisconsin.    Foreign distribution to Canada, Asia, Europe, and Australia.

## Key facts

- **Recall number:** Z-1352-2019
- **Recalling firm:** Moller Vital
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2019-02-04
- **Report date:** 2019-05-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Gjovik, Norway

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1352-2019

## Citation

> AI Analytics. FDA recall Z-1352-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-1352-2019. Source: US FDA. Licensed CC0.

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