Recall Z-2319-2008 ยท FSA Lift, Patient, Non-Ac-Powered
Liko AB
Universal SlingBar 450 with Quick-release Hook Product Number: 3156085 Used in combination with all lifts from Liko, i.e. mobile lifts and overhead lifts
| Date | Sep 20, 2008 (initiated Jul 1, 2008) |
| Status | Terminated |
| Reason | 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. |
| Root cause | Component design/selection |
| Action | 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. |
| Distribution | Nationwide |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
This recall record lists no 510(k) number.