Likorall Overhead Lifts
Medical device recall Z-0151-2027. Published in FDA’s Enforcement Report on Oct 21, 2026.
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 Oct 21, 2026. Copied from openFDA on Oct 27, 2026.
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 II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
Potential issue involving motor shaft breakage combined with reduced performance of the Single Fault Safety (SFS) system may lead to instances where the lift strap lowers more quickly than expected during use. Patients are at some risk for injury if a significant fall/drop were to occur due to this issue.
FDA, Device recall enforcement reports. Released Oct 27, 2026. Updated weekly.
Which ones are recalled?
Likorall Overhead Lifts Product Code: 3121001 Product Description: LIKORALL 200 Product Code: 3122005 Product Description: LIKORALL 242 ES, NATURAL Product Code: 3122005NA Product Description: LIKORALL 242 ES, NATURAL Product Code: 3122006 Product Description: LIKORALL 242 ES, WHITE Product Code: 3122006NA Product Description: LIKORALL 242 ES, WHITE Product Code: 3122007 Product Description: LIKORALL 242 ES R2R, NATURAL Product Code: 3122007NA Product Description: LIKORALL 242 ES R2R, NATURAL Product Code: 3122008 Product Description: LIKORALL 242 ES R2R, WHITE Product Code: 3122008NA Product Description: LIKORALL 242 ES R2R, WHITE Product Code: 3122009 Product Description: LIKORALL 242 S, NATURAL Product Code: 3122009NA Product Description: LIKORALL 242 S, NATURAL Product Code: 3122010 Product Description: LIKORALL 242 S, WHITE Product Code: 3122011 Product Description: LIKORALL 242 S R2R, NATURAL Product Code: 3122011NA Product Description: LIKORALL 242 S R2R, NATURAL Product Code: 3122012 Product Description: LIKORALL 242 S R2R, WHITE Product Code: 3122012NA Product Description: LIKORALL 242 S R2R, WHITE Product Code: 3122501 Product Description: LIKORALL 250 ES, NATURAL Product Code: 3122501NA Product Description: LIKORALL 250 ES, NATURAL Product Code: 3122502 Product Description: LIKORALL 250 ES, WHITE Product Code: 3122502NA Product Description: LIKORALL 250 ES, WHITE Product Code: 3123001 Product Description: LIKORALL 243 ES Product Code: 3123001NA Product Description: LIKORALL 243 ES Product Code: 3123002 Product Description: LIKORALL 243 ES, WHITE Product Code: 3123002NA Product Description: LIKORALL 243 ES, WHITE Product Code: 3124050 Product Description: LIKORALL 250 S, IRC
FDA, Device recall enforcement reports. Released Oct 27, 2026. Updated weekly.
Codes to check against yours
Product Code: 3121001 Product Description: LIKORALL 200 Lot/Serial Number: Intervals: 8400054-8450499 and 9000000-9000999 UDI-DI Number: 00887761981911 Product Code: 3122005 Product Description: LIKORALL 242 ES, NATURAL Lot/Serial Number:…
Every code shown here, 1,994 characters
Product Code: 3121001 Product Description: LIKORALL 200 Lot/Serial Number: Intervals: 8400054-8450499 and 9000000-9000999 UDI-DI Number: 00887761981911 Product Code: 3122005 Product Description: LIKORALL 242 ES, NATURAL Lot/Serial Number: Greater than or equal to 8104548 UDI-DI Number: 00887761979710 Product Code: 3122005NA Product Description: LIKORALL 242 ES, NATURAL Lot/Serial Number: Interval: 429087-431032 UDI-DI Number: 00887761979727 Product Code: 3122006 Product Description: LIKORALL 242 ES, WHITE Lot/Serial Number: Greater than or equal to: 8101715 UDI-DI Number: 00887761979734 Product Code: 3122006NA Product Description: LIKORALL 242 ES, WHITE Lot/Serial Number: Interval: 429186-431035 UDI-DI Number: 00887761979741 Product Code: 3122007 Product Description: LIKORALL 242 ES R2R, NATURAL Lot/Serial Number: Greater than or equal to: 8104481 UDI-DI Number: 00887761979758 Product Code: 3122007NA Product Description: LIKORALL 242 ES R2R, NATURAL Lot/Serial Number: Interval: 429041-430984 UDI-DI Number: 00887761979765 Product Code: 3122008 Product Description: LIKORALL 242 ES R2R, WHITE Lot/Serial Number: Greater than or equal to: 8100815 UDI-DI Number: 00887761979772 Product Code: 3122008NA Product Description: LIKORALL 242 ES R2R, WHITE Lot/Serial Number: Interval: 429081-431018 UDI-DI Number: 00887761979789 Product Code: 3122009 Product Description: LIKORALL 242 S, NATURAL Lot/Serial Number: Greater than or equal to: 8000235 UDI-DI Number: 00887761979796 Product Code: 3122009NA Product Description: LIKORALL 242 S, NATURAL Lot/Serial Number: Interval: 286125-289686 UDI-DI Number: 00887761979802 Product Code: 3122010 Product Description: LIKORALL 242 S, WHITE Lot/Serial Number: Greater than or equal to: 8000114 UDI-DI Number: 00887761979819 Product Code: 3122011 Product Description: LIKORALL 242 S R2R, NATURAL Lot/Serial Number: Greater than or equal to: 8001716 UDI-DI Number: 00887761979444 Product Code: 3122011NA Product Description: LIKORALL 242 S R2R,…
FDA’s list runs to 3,657 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 - US Nationwide distribution including in the states of Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, Wisconsin, and Wyoming. International distribution in pending.
The states and territories these words name
49 states and territories.
Every one of them
- Alaska
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- Delaware
- Florida
- Georgia
- Hawaii
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Maine
- Michigan
- Minnesota
- Missouri
- Mississippi
- Montana
- North Carolina
- North Dakota
- Nebraska
- New Hampshire
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- Washington
- Wisconsin
- West Virginia
- Wyoming
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?
Ongoing, in FDA’s file.
“A recall which is currently in progress.”
openFDA, on “On-Going”, 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 Sep 14, 2026.
- FDA classified it on Oct 13, 2026.
- FDA’s Enforcement Report published it on Oct 21, 2026.
FDA, Device recall enforcement reports. Released Oct 27, 2026. Updated weekly.
Who is recalling it?
- Baxter Healthcare Corporation, of Deerfield, IL.
- 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 27, 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 3,657 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 27, 2026 and checked Oct 27, 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 27, 2026.