FDA Device recall Z-0925-2021
Liko Multirall 200 overhead lift- overhead lift is a general-purpose lift with the intended use in healthcare, intensive care and rehabilit…
- FDA Device
- Class I
- terminated
- Published 2021-02-10
On 2021-02-10 the FDA classified a Class I recall of Liko Multirall 200 overhead lift- overhead lift is a general-purpose lift with the intended use in healthcare, intensive care and rehabilit… by Hill Rom, citing multirall Q-link strap lock has not been fully engaged in the S65 rail carriage hook by user, leading to the Multirall lift becoming detached from the rail system, potentially res….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0925-2021 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2020-12-18 |
| Published | 2021-02-10 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Hill Rom |
| Distribution | US |
Product
Liko Multirall 200 overhead lift- overhead lift is a general-purpose lift with the intended use in healthcare, intensive care and rehabilitation. Affected devices: Liko Multirall 200 (product number 3130001) Universal SlingBar 450 R2R (product number 3156095) Universal SlingBar 350 R2R (product number 3156094) Carriage D45 with Double Hook (product number 3136100) Extension belt 300-400 mm (product number 3136226) Extension belt 400-600 mm (product number 3136227) Extension belt 600-1000 mm (product number 3136228) Extension belt 1000-1400mm (product number 3136229)
Reason
Multirall Q-link strap lock has not been fully engaged in the S65 rail carriage hook by user, leading to the Multirall lift becoming detached from the rail system, potentially resulting in the fall of both the lift motor and the patient
Identifiers
| code_info | Serial Numbers: All Multirall 200 with serial number < 6511935 (all devices manufactured before 24SEP2019) Except for…Serial Numbers: All Multirall 200 with serial number < 6511935 (all devices manufactured before 24SEP2019) Except for the reworked serial numbers listed below: 6511692, 6511701, 6511704, 6511706, 6511713, 6511707, 6511709, 6511719, 6511708, 6511689, 6511702, 6511703, 6511691, 6511694, 6511714, 6511690, 6511383, 6511358, 6511375, 6511386, 6511380, 6511376, 6511365, 6511379, 6511333, 6511356, 6511362, 6511363, 6511357, 6511359, 6511377, 6511378, 6511361, 6511329, 6511327, 6511318, 6511320, 6511793, 6511319, 6511328, 6511336, 6511324, 6511326, 6511325, 6511323, 6511321, 6511334, 6511310, 6511189, 6511312, 6511787, 6511792, 6511748, 6511802, 6511799, 6511797, 6511796, 6511800, 6511185, 6511770, 6511805, 6511810, 6511803, 6511807, 6511772, 6511757, 6511806, 6511804, 6511811, 6511801 EXPANDED RECALL 3/17/2021: The following additional serial numbers have been determined to be affected as a Q-Link 1 Service part may been ordered for it: 651338 6512166 6512306 6512418 6512461 6512 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0925-2021%22
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