Recall Z-0105-2019 ยท FSA Lift, Patient, Non-Ac-Powered
Liko AB
Multirall(TM) 200Liko Strap Gripper P/N 3136250 overhead lift for patient transfer situations.
| Date | Jul 17, 2018 |
| Status | Terminated |
| Reason | The products manufactured on 5/5/17 may be assembled incorrectly. If the incorrectly assembled products is used for patient transport, this could allow the patient to fall, resulting in potential injury to the patient. |
| Root cause | Storage |
| Action | The customer was contacted via telephone on 7/17/18 to notify them of the recall. An Urgent Field Safety Notice notification letter was sent to the customer on 7/19/18. |
| Quantity | 2 |
| Distribution | The products were distributed to the following US states: OH. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
This recall record lists no 510(k) number.