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Type of Product Medical Device
TGA Recall Reference RC-2015-RN-00893-1
Product Name/Description Liko Viking mobile lifts
(Liko Lift devices are intended to lift and/or transfer the patients between floors, beds, chairs, etc, from one position to another.)

Viking M
Model 2040035 (S/N 9 200 000 – 9 201 689)
Model 2040015 (S/N 7 500 401 – 7 568 899)
Model 2040005 (S/N 7 100 101 – 7 200 200)

Viking L
Model 2040004 (S/N 7 200 201 – 7 300 300)

Viking XL or Viking 300 Lift
Model 2040003 (S/N 801 301 – 804 999)

ARTG Number: 161863
Recall Action Level Hospital
Recall Action Classification Class II
Recall Action Commencement Date 10/09/2015
Responsible Entity Hill-Rom Pty Ltd
Reason/Issue Hill-Rom has received 9 complaints where it has been described that the lift arm drifted down suddenly on certain Viking mobile lifts. These reports have been connected to users who raise the lift arm assembly manually.

The lift arm assembly is intended to only be raised by the actuator (lift motor). If the lift arm assembly is manually raised, the actuator can become damaged and get stuck in the highest position. When the actuator is stuck, the lift cannot be raised or lowered by the lift motor.

Hill-Rom requests customers do not raise the lift arm manually since the lifting actuator can become stuck and/or become damaged.
Recall Action Recall for Product Correction
Recall Action Instructions Hill-Rom is conducting a correction in two phases.
Phase 1 will be this letter and information for you to update the Instruction Guides. Phase 2 will include the physical inspection of potentially affected devices. If there is damage to the actuator consistent with manually lifting, the actuator will be replaced by Hill-Rom.

This action has been closed out on 24/10/2018
Contact Information 1800 445 576 - Technical Support