Likorall Overhead Lifts Product Code: 3121001 Product Description: LIKORALL 200 Product Code: 3122005 Product De
Summary
The FDA issued a Class II for Likorall Overhead Lifts Product Code: 3121001 Product Description: LIKORALL by Baxter Healthcare Corporation. Reason: Potential issue involving motor shaft breakage combined with reduced performance of the Single Fault Safety (SFS) system may lead to instances where t.
Details
Source
Device Recall
External ID
Z-0151-2027
Action Date
2026-10-21
Status
Ongoing
Category
device
Product Description
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
Lot/Code Info: 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, NATURAL Lot/Serial Number: Interval: 286040-289602 UDI-DI Number: 00887761979451 Product Code: 3122012 Product Description: LIKORALL 242 S R2R, WHITE Lot/Serial Number: Greater than or equal to: 8014169 UDI-DI Number: 00887761979468 Product Code: 3122012NA Product Description: LIKORALL 242 S R2R, WHITE Lot/Serial Number: Interval: 286047-289640 UDI-DI Number: 00887761979475 Product Code: 3122501 Product Description: LIKORALL 250 ES, NATURAL Lot/Serial Number: Greater than or equal to: 8300562 UDI-DI Number: 00887761979482 Product Code: 3122501NA Product Description: LIKORALL 250 ES, NATURAL Lot/Serial Number: Interval: 6604187-6606919 UDI-DI Number: 00887761979499 Product Code: 3122502 Product Description: LIKORALL 250 ES, WHITE Lot/Serial Number: Greater than or equal to: 8300004 UDI-DI Number: 00887761979505 Product Code: 3122502NA Product Description: LIKORALL 250 ES, WHITE Lot/Serial Number: Interval: 6604051-6606836 UDI-DI Number: 00887761979512 Product Code: 3123001 Product Description: LIKORALL 243 ES Lot/Serial Number: Greater than or equal to: 8200065 UDI-DI Number: 00887761979529 Product Code: 3123001NA Product Description: LIKORALL 243 ES Lot/Serial Number: Interval: 362939-368654 UDI-DI Number: 00887761979536 Product Code: 3123002 Product Description: LIKORALL 243 ES, WHITE Lot/Serial Number: Greater than or equal to: 8206060 UDI-DI Number: 00887761979543 Product Code: 3123002NA Product Description: LIKORALL 243 ES, WHITE Lot/Serial Number: Interval: 368113-368658 UDI-DI Number: 00887761979550 Product Code: 3124050 Product Description: LIKORALL 250 S, IRC Lot/Serial Number: Interval: 2108-24074 UDI-DI Number: 00887761979567
Reason for Recall
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.
Distribution
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.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-09-14
Company
Deerfield, IL
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 150 device recalls issued in the same week, part of 446 device-related FDA actions this month.
Baxter Healthcare Corporation has 335 FDA actions in our database, including 312 recalls and 23 clearances.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Baxter Healthcare Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Baxter Healthcare Corporation have FDA actions?
Baxter Healthcare Corporation has 335 FDA actions in our database, including 312 recalls and 23 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-0151-2027" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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