# FDA recall Z-0105-2019

> **Liko AB** · Class II · device recall initiated 2018-07-17.

## Product

Multirall(TM) 200Liko Strap Gripper P/N 3136250 overhead lift for patient transfer situations.

## Reason for recall

The products manufactured on 5/5/17 may be assembled incorrectly.  If the incorrectly assembled products is used for patient transport, this could allow the patient to fall, resulting in potential injury to the patient.

## Distribution

The products were distributed to the following US states: OH.

## Key facts

- **Recall number:** Z-0105-2019
- **Recalling firm:** Liko AB
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-07-17
- **Report date:** 2018-10-24
- **Termination date:** 2019-04-19

- **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-0105-2019

## Citation

> AI Analytics. FDA recall Z-0105-2019. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0105-2019. Source: US FDA. Licensed CC0.

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