Recall Z-0277-06 ยท FSA Lift, Patient, Non-Ac-Powered
Liko, Inc.
UNO 102 Patient Lift
| Date | Dec 13, 2005 (initiated Nov 14, 2005) |
| Status | Terminated |
| Reason | Incorrect length leg pin bolts may cause patient lift failures |
| Root cause | Other |
| Action | Liko Inc. initiated the recall to Distributors of the Recall on 11/14/05 via UPS. Direct customers will be notified by letter on /about 12/1/05. |
| Quantity | 663 units |
| Distribution | Nationwide |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
This recall record lists no 510(k) number.