Liko AB recalls Multirall(TM) 200Liko Strap Gripper P/N 3136250 overhead lift for patient transfer situations.

Recall date

July 17, 2018

Source

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

Recall number

Z-0105-2019

FDA classification

Class II

Brand / firm

Liko AB

Sold / distributed

The products were distributed to the following US states: OH.

Why it was recalled

The products manufactured on 5/5/17 may be assembled incorrectly. If the incorrectly assembled products is used for patient transport, this could allow the patient to fall, resulting in potential injury to the patient.

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

What was recalled

Multirall(TM) 200Liko Strap Gripper P/N 3136250 overhead lift for patient transfer situations.