FDAJuly 17, 2018device
Multirall(TM) 200Liko Strap Gripper P/N 3136250 overhead lift for patient transfer situations.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
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.
What to do
FDA enforcement status: Terminated
Brands named
liko abliko
Recall history
No related federal recalls on record for this brand yet.
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