Liko AB: Medical Device Recall in 2018 - (Recall #: Z-0105-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: July 17, 2018

Date Posted: October 24, 2018

Recall Number: Z-0105-2019

Event ID: 80911

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.

Status: Terminated

Product Quantity: 2

Code Information:

Part Number 3136250, the manufacturing date is on the right side of the label listed as 2017-05-05.

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated