Hill-Rom Liko Multirall 200 Lift Recall: Q-Link Strap Lock May Detach Causing Falls
Hill-Rom recalls Liko Multirall 200 overhead lifts with serial numbers < 6511935 (made before Sep 24, 2019) due to Q-Link strap lock not engaging properly, risking patient and lift detachment.
Stop using this now
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
Contact the company
What happened, in plain English
Hill-Rom recalls Liko Multirall 200 overhead lifts with serial numbers below 6511935 (manufactured before September 24, 2019) because the Q-Link strap lock may not stay engaged, causing the lift to detach from the rail system and potentially fall, risking injury to both the patient and the lift. Read more at govinfonow.com/recall/63638-hill-rom-liko-multirall-200-lift-recall-q-link-strap.
Source Summary by GovInfoNow · govinfonow.com/recall/63638-hill-rom-liko-multirall-200-lift-recall-q-link-strap · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0925-2021
Cite this page
“Hill-Rom Liko Multirall 200 Lift Recall: Q-Link Strap Lock May Detach Causing Falls.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/63638-hill-rom-liko-multirall-200-lift-recall-q-link-strap. Based on FDA recall #Z-0925-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0925-2021%22&limit=1).
Why it’s dangerous
The Q-Link strap lock may not stay fully engaged in the S65 rail carriage hook, causing the lift to become detached from the rail system. If the lift detaches, it could fall, potentially causing injury to the patient and the lift itself.
Who’s affected
Healthcare facilities using Liko Multirall 200 overhead lifts with serial numbers below 6511935 (made before September 24, 2019) are most at risk, as the device is used for patient lifting in hospitals and rehabilitation centers.
How to tell if you have this one
Check if your Liko Multirall 200 overhead lift has a serial number below 6511935 (all devices manufactured before September 24, 2019). The recall includes specific extension belts and carriage components with matching serial numbers.
- Brand
Hill-Rom- Category
Medical device
What to do — step by step
Stop Using It Now
Immediately stop using the Liko Multirall 200 overhead lift if it has a serial number below 6511935 (manufactured before September 24, 2019).
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “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.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA terminated this recall 2.8 years after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
What models are affected by this recall?
Liko Multirall 200 (product number 3130001), Universal SlingBar 450 R2R (3156095), Universal SlingBar 350 R2R (3156094), Carriage D45 with Double Hook (3136100), and specific extension belts with serial numbers below 6511935.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-0925-2021 (December 18, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0925-2021 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.