Handicare AB recalls EVA Floor Lifts, Model Numbers: 400, 450, 600

Recall date

June 15, 2016

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-1943-2020

FDA classification

Class II

Brand / firm

Handicare AB

Sold / distributed

US and Mexico

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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