Liko Multirall 200 overhead lift- overhead lift is a general-purpose lift with the intended use in…
Medical device recall Z-0925-2021. Published in FDA’s Enforcement Report on Feb 10, 2021.
- FDA Class I
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Feb 10, 2021. Copied from openFDA on Oct 20, 2026.
- Class I FDA’s most serious class (needs attention)
- Terminated its status, in FDA’s file
- Nationwide FDA’s word for where it went
- 10470 units Expanded Recall: 154 units how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class I, the most serious of FDA’s three classes.
“Dangerous or defective products that predictably could cause serious health problems or death. Examples include: food found to contain botulinum toxin, food with undeclared allergens, a label mix-up on a lifesaving drug, or a defective artificial heart valve.”
openFDA, in plain words, its enforcement report fields.
“Class I is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.”
FDA’s rule, 21 CFR 7.3(m)(1), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
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
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
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)
10470 units Expanded Recall: 154 units, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
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,…
Every code shown here, 1,999 characters
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…
FDA’s list runs to 2,174 characters. The first part is shown; the rest is on FDA’s record.
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
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.
These words name no state.
What FDA means by nationwide
“The term “nationwide” is defined to mean the fifty states or a significant portion. Note that subsequent distribution by the consignees to other parties may not be included.”
openFDA, its enforcement report fields.
The words say it went outside the United States too.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Terminated, in FDA’s file.
“FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard.”
openFDA, on “Terminated”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Dec 18, 2020.
- FDA classified it on Jan 29, 2021.
- FDA’s Enforcement Report published it on Feb 10, 2021.
- FDA terminated it on Sep 26, 2023.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Hill-Rom, Inc., of Batesville, IN.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Letter.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- FDA’s list of codes runs to 2,174 characters; the first part is shown here, and the rest is on FDA’s record.
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
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U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.