FDA recall Z-0105-2019

Product

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

Reason for recall

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.

Distribution

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

Key facts

Status

Terminated

Initiation date

2018-07-17

Report date

2018-10-24

Termination date

2019-04-19

Voluntary/Mandated

Voluntary: Firm initiated

Location

Lulea, N/A, Sweden

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0105-2019