# FDA recall Z-2753-2018

> **Handicare Usa Inc** · Class II · device recall initiated 2017-11-03.

## Product

Handicare P600 Series Patient Lift  Product Usage:  A device used to lift and transport a patient from one place to another.

## Reason for recall

Premature strap wear and breakage at maximum weight conditions (625 lbs.).

## Distribution

Worldwide Distribution - US Nationwide in the states of AK, CA, CT, DE, GA, IA, IL, KY, LA, MA, ME, MI, MN, MO, NE, NV, NY, OH, OR, PA, RI, TN, TX, WI, and Puerto Rico and the countries of Canada and Australia,

## Key facts

- **Recall number:** Z-2753-2018
- **Recalling firm:** Handicare Usa Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-11-03
- **Report date:** 2018-08-29
- **Termination date:** 2020-07-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Maryland Heights, MO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2753-2018

## Citation

> AI Analytics. FDA recall Z-2753-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2753-2018. Source: US FDA. Licensed CC0.

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