Recall Z-0875-05 ยท FNG Lift, Patient, Ac-Powered
Liko, Inc.
UNO 102 EM/EE/ES Patient Lift
| Date | Jun 8, 2005 (initiated Sep 24, 2004) |
| Status | Terminated |
| Reason | Incorrect length support screws may cause patient lift failure |
| Root cause | Other |
| Action | Liko notified Peridot Group by letter dated 9/29/04 of the recall. All Canadian distributors, including Peridot, will contact and inspect and replace bolts at user sites. |
| Quantity | 21 units |
| Distribution | Canada |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
This recall record lists no 510(k) number.