RecallDepth

EVA Floor Lifts, Model Numbers: 400, 450, 600

Company
Handicare Ab Maskinvagen
Recall Initiated
June 15, 2016
Recall Number
Z-1943-2020
Quantity
997 units

Reason for Recall

After feedback from customers and internal suspicion, Handicare has become aware that abnormal use of Eva-lifts could lead to a deterioation in the joint of the liftarm. This could lead to injury if the joint breaks. All lifts must therefore be checked and reported back to the manuafacturer.

Distribution

US and Mexico

Lot / Code Info

All affected models

Root Cause

Device Design

Action Taken

The firm notified their consignees on 06/15/2016 by email. The notice explained the issue of wear in the joint of the lift arm due to abnormal use in heavy loads and/or many lifts. The consignee was directed to inspect the lifts in order to identify gaps and/or cracks and to report to the local Handicare sales representative and to Handicare. On April 4, 2019, the firm sent a reminder notice on 04/04/2019

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