Universal SlingBar 350 with Quick-release Hook Product Number: 3156084 Used in combination with all lifts from Liko, i.e
FDA device recall Z-2318-2008 · posted 2008-09-20 · Terminated
Recall details
- Recalling firm
- Liko AB
- Reason for recall
- A component securing the Universal SlingBar to the patient lift, may experience a nut unthreading resulting in the sling bar detaching from the lift causing the patient to fall.
- Action taken
- Liko North America ,the US Distributor, notified accounts by letter dated June 30, 2008 and provided a Field Safety Notice with Safety Inspection Procedures to performed on the lift prior to use. Replacement slingbars are being provided. If you have questions, contact the Liko product distributor in your country. Contact information can be found at www.liko.com/int/distributors.asp.
- Root cause
- Component design/selection
- Status
- Terminated
- Product code
- FSA
- Distribution
- Nationwide
- Date initiated
- 2008-07-01
- Date posted
- 2008-09-20
- Date terminated
- 2015-07-17
- Location
- Lulea, Sweden
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