Recall Z-0790-06 ยท FSA Lift, Patient, Non-Ac-Powered
Liko, Inc.
Liko Universal Slingbar 450 (aluminum) used with the Viking M Patient Lift
| Date | Apr 26, 2006 (initiated Jan 9, 2006) |
| Status | Terminated |
| Reason | The swivel adapter which is mounted directly above the slingbar's split center bolt could be removed and allow the slingbar to be improperly mounted directly into the aluminum link arm. This could cause an unsafe transfer. Patient may fall. |
| Root cause | Other |
| Action | Liko notified Distributors of the recall by letter on 1/9/06 via UPS and provided replacement Slingbars Version 2. Expanded Recall: On 6/20/06, Liko sent a 2nd recall letter expanding the recall to additonal serial numbers via Certified Mail. |
| Quantity | 67 units |
| Distribution | IL, MA, MO, PA, TN, |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
This recall record lists no 510(k) number.