Reported Oct 21, 2020 · Terminated
SwiftHook sold as the following: a. Individually as SwiftHook b. Included with Vega505EE mobile lifts Product Usage:…
Handicare AB
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Handicare AB · Maskinvagen 17 · Lulea, N/A · N/A
Is this the product you have?
- SwiftHook sold as the followinga. Individually as SwiftHook b. Included with
- Vega505EE mobile lifts Product UsageThe mobile lifts are intended to assist people with functional impairments in scenarios involving physical positioning
- Lot codes and dates
3 of 3 products
Products covered by this recall Model / number Barcodes Product as published 70200008— 60600003— — 733176902042266031185404226603118560422Serial Numbers 660311979, 660311759, 010733176902042221660312235, 660311299, 660312299 660311338, 7331769020422, 660311817,660311846, 660311847, 660311848, 6603118540422, 660311855, 6603118560422, 660311849, 660311850, 660311851, 660311852, 660311877, 660311878, 660311880, 660311941, 660311942, 660311968, sales order number 100931 (serial number could not be located) - Amount recalled
- 6716 units (585 in US; 6131 in OUS)
Where it was sold
Why it was recalled
Carry bar may detach during use of mobile lifts and ceiling lifts equipped with the Swifthook component.
This product could cause temporary or reversible health problems — stop using it.
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