FDAMarch 20, 2015device
Viking M, L, and XL Mobile Lifts. Non-AC-powered patient lift.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Complaints (including one reported death) allegedly of the lift arm drifting down suddenly. If the lift arm assembly is manually lifted, the actuator can become damaged and get stuck in the highest position. If a patient is lifted into the sling while the actuator is stuck, there is a potential risk of a free fall of the patient, resulting in minor or potentially catastrophic injuries.
What to do
FDA enforcement status: Terminated
Brands named
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Recall history
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