Liko AB Uno Lifts, Powered (non-AC) Patient Lift: Uno 100 EM/EE: S/N 7090001 through 7096200 Uno 101: S/N 10001 through
FDA device recall Z-0605-2009 · posted 2009-01-27 · Terminated
Recall details
- Recalling firm
- Liko North America Inc
- Reason for recall
- Actuator of the lift has the potential to separate when the upper arm is fully extended.
- Action taken
- Hill Rom notified customers with a Field Safety Notice, dated December 5, 2008 to notify customers of the issue, potential risks, and to inspect units per their instructions and remove units from service if the unit fails inspection. Hill-Rom will provide a permanent fix, using an "OuterTube" to be placed on all units.
- Root cause
- Process control
- Status
- Terminated
- Product code
- FSA
- Quantity affected
- 24070 total units
- Distribution
- Worldwide Distribution --- including USA and country of Canada.
- Date initiated
- 2008-11-11
- Date posted
- 2009-01-27
- Date terminated
- 2016-02-04
- Location
- Franklin, MA
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