FDA Device recall Z-0105-2019
Multirall(TM) 200Liko Strap Gripper P/N 3136250 overhead lift for patient transfer situations
- FDA Device
- Class II
- terminated
- Published 2018-10-24
On 2018-10-24 the FDA classified a Class II recall of Multirall(TM) 200Liko Strap Gripper P/N 3136250 overhead lift for patient transfer situations by Liko Ab, citing 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, result….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0105-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-07-17 |
| Published | 2018-10-24 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Liko Ab |
| Distribution | OH |
Product
Multirall(TM) 200Liko Strap Gripper P/N 3136250 overhead lift for patient transfer situations.
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.
Identifiers
| code_info | Part Number 3136250, the manufacturing date is on the right side of the label listed as 2017-05-05. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0105-2019%22
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