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Recall Observatory FDA recall evidence

Device product

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

Z-0105-2019

July 17, 2018

Class II

Product summary

Firm
Liko AB
Event
Event 80911
Status
Terminated
Classification
Class II
Quantity
2
Official record key
device-enforcement:Z-0105-2019

Official wording

Reason: 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.

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.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.