Data Foundry

Medical device recalls 2020

SwiftHook sold as the following: a — Class II medical device recall Z-0096-2021

Terminated recall by Handicare AB, reported 2020-10-21, distributed nationwide. Carry bar may detach during use of mobile lifts and ceiling lifts equipped with the Swifthook component.

Recall numberZ-0096-2021
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmHandicare AB, Lulea, N/A, Sweden
Recall initiated2020-08-21
Classified2020-10-09
Reported by FDA2020-10-21
Terminated2023-01-30
DistributedNationwide (US)
Countries outside the USAE, AU, BE, CA, CL, DE, DK, ES, FI, GB, IE, IL, IS, JP, LT, MY, NL, NO, NZ, PL, PT, QA, SA, SE, TW
Quantity6,716 units
Reason classesdevice malfunction
UPC / GTIN / UDI-DI07331769020422
Serial numbers010733176902042221660312235, 660311299, 660311338, 660311759, 660311817, 660311846, 660311847, 660311848, 660311849, 660311850, 660311851, 660311852, 6603118540422, 660311855, 6603118560422, 660311877, 660311878, 660311880, 660311941, 660311942, 660311968, 660311979, 660312299, 7331769020422
Model numbers60600003, 70200008

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0096-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.