# FDA recall Z-0096-2021

> **Handicare AB** · Class II · device recall initiated 2020-08-21.

## Product

SwiftHook sold as the following:  a. Individually as SwiftHook  b. Included with Vega505EE mobile lifts  Product Usage: The mobile lifts are intended to assist people with functional impairments in scenarios involving physical positioning.

## Reason for recall

Carry bar may detach during use of mobile lifts and ceiling lifts equipped with the Swifthook component.

## Distribution

Worldwide distribution - US Nationwide distribution including in the states of CA, IL, MD, MI, MN, NH, NJ, NY, ON, PA, TX, VA, WA, WI and the countries of Australia, Belgium, Canada, Chile, Denmark, Finland, Germany, Iceland, Ireland, Israel, Japan, Lithuania/ Lathvia, Malaysia, New Zealand, Norway, Poland, Portugal, Qatar, Saudi Arabia, Spain, Sweden, Taiwan  the Netherlands, UAE, UK.

## Key facts

- **Recall number:** Z-0096-2021
- **Recalling firm:** Handicare AB
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-08-21
- **Report date:** 2020-10-21
- **Termination date:** 2023-01-30

- **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-0096-2021

## Citation

> AI Analytics. FDA recall Z-0096-2021. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-0096-2021. Source: US FDA. Licensed CC0.

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