# FDA recall Z-0014-2018

> **Handicare AB** · Class II · device recall initiated 2016-07-28.

## Product

Carina Mobile Lifts, Models:    a) Carina350EM, REF 6060011  b) Carina350EML, REF 60600012  c) Carina350EE, REF 60600009

## Reason for recall

A limited amount of Carina mobile lifts have been delivered with a too small locking pin. If a locking pin  smaller than the correct size is mounted on the Carina mobile lift, the locking pin is likely to cause  increased wear on the plastic bushings. In case of continued use, these components may cause wear on the metal of the piston rod eye.

## Distribution

OH, PA, MD

## Key facts

- **Recall number:** Z-0014-2018
- **Recalling firm:** Handicare AB
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2016-07-28
- **Report date:** 2017-10-18
- **Termination date:** 2018-12-17

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0014-2018

## Citation

> AI Analytics. FDA recall Z-0014-2018. Retrieved 2026-07-18 from https://api.ai-analytics.org/recall/Z-0014-2018. Source: US FDA. Licensed CC0.

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