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.
Reported: October 21, 2020 Initiated: August 21, 2020 #Z-0096-2021
Product Description
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.
Details
- Recalling Firm
- Handicare AB
- Units Affected
- 6716 units (585 in US; 6131 in OUS)
- 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.
- Location
- Lulea, N/A
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Handicare AB. Units affected: 6716 units (585 in US; 6131 in OUS).
Why was this product recalled? ▼
Carry bar may detach during use of mobile lifts and ceiling lifts equipped with the Swifthook component.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 21, 2020. Severity: Moderate. Recall number: Z-0096-2021.
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