CLASS I Device recall · Reported 10 Feb 2021 · FDA Enforcement Report
Liko Multirall 200 overhead lift- overhead lift recalled by Hill-Rom
Hill-Rom is recalling Liko Multirall 200 overhead lift- overhead lift is a general-purpose lift with the, distributed nationwide in the US. The recall was initiated on 18 Dec 2020 and the FDA has classified it as Class I.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-0925-2021
- FDA event ID
- 87053
- Recalling firm
- Hill-Rom, Batesville, IN
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 18 Dec 2020
- FDA classified
- 29 Jan 2021
- Reported
- 10 Feb 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 18 Dec 2020 | Recall initiated by company | |
| 29 Jan 2021 | Classified by FDA | +42 days |
| 10 Feb 2021 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
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
Product as listed by the FDA
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)
Where it was distributed
Worldwide distribution: US (Nationwide) and countries of::AT, AU, BR, CA, CH, CZ, DE, DK, ES, FI, FR, GB, GR, IE, IL, IS, IT, JP, LV, NL, NO, NZ, SE & SK.
Questions about this recall
Why was it recalled?
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
Which lots are affected?
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 6512524 6512548 6512684 6512822 6511935 6512188 6512319 6512420 6512484 6512525 6512549 6512685 6512823 6511962 6512194 6512321 6512421 6512486 6512528 6512553 6512686 6512825 6511964 6512195 6512330 6512424 6512487 6512529 6512562 6512687 6512829 6511968 6512202 6512336 6512425 6512488 6512530 6512581 6512688 6512831 6511970 6512204 6512338 6512429 6512493 6512531 6512582 6512691 6512833 6512014 6512206 6512340 6512430 6512497 6512532 6512583 6512692 6512838 6512015 6512214 6512341 6512436 6512500 6512533 6512589 6512694 6512839 6512106 6512220 6512342 6512437 6512501 6512534 6512619 6512695 6512840 6512107 6512221 6512345 6512440 6512503 6512535 6512621 6512696 6512882 6512119 6512224 6512356 6512441 6512506 6512540 6512623 6512697 6512886 6512125 6512233 6512406 6512442 6512507 6512542 6512636 6512780 6512932 6512129 6512240 6512408 6512443 6512508 6512543 6512637 6512787 6512943 6512134 6512248 6512410 6512444 6512509 6512544 6512668 6512788 6513042 6512150 6512255 6512412 6512446 6512510 6512545 6512681 6512811 6513043 6512154 6512262 6512415 6512448 6512514 6512546 6512682 6512820 6513089 6512157 6512296 6512417 6512449 6512517 6512547 6512683 6512821 6513092 6542422
Where was it sold?
Worldwide distribution: US (Nationwide) and countries of::AT, AU, BR, CA, CH, CZ, DE, DK, ES, FI, FR, GB, GR, IE, IL, IS, IT, JP, LV, NL, NO, NZ, SE & SK.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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