Likorall Overhead Lifts Product Code: 3121001 Product Description: LIKORALL 200 Product Co...
FDA Device Recall #Z-0151-2027 - Class II, September 14, 2026
Recall Summary
| Recall Number | Z-0151-2027 |
| Classification | Class II - Moderate risk |
| Date Initiated | September 14, 2026 |
| Status | Ongoing |
| Voluntary | Voluntary: Firm initiated |
Recalling Firm
| Firm | Baxter Healthcare Corporation |
| Location | Deerfield, IL |
| Product Type | Devices |
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
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 Pattern
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.
Lot / Code Information
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
Other Recalls from Baxter Healthcare Corporation
| Recall # | Classification | Product | Date |
|---|---|---|---|
| Z-3262-2026 | Class II | PRO+ MRS SURFACE FOR VERSACARE, mattress with A... | Aug 18, 2026 |
| Z-3264-2026 | Class II | PRO+ 40" MRS SURFACE, mattress with Advanced Mi... | Aug 18, 2026 |
| Z-3263-2026 | Class II | PRO+ 36" MRS SURFACE, mattress with Advanced Mi... | Aug 18, 2026 |
| Z-3066-2026 | Class II | Baxter Novum IQ Syringe Pump, Loaner, Model Num... | Aug 11, 2026 |
| Z-3065-2026 | Class II | Baxter Novum IQ Syringe Pump, Model Number 4080... | Aug 11, 2026 |
Frequently Asked Questions
Contact your healthcare provider and the device manufacturer immediately. Check whether your specific model number and lot number are included in the recall scope. For external devices, stop using the affected product and arrange a replacement. For implanted devices, do not panic, removal is typically not required unless the risk assessment clearly indicates it. Your physician will guide you based on your individual clinical situation and the FDA's recommended actions. Report any adverse effects you may have experienced to FDA MedWatch at 1-800-FDA-1088.
Class I recalls indicate a reasonable probability of serious adverse health consequences or death from the defect. Class II recalls involve products that may cause temporary or medically reversible adverse health consequences, or where serious consequences are remote. Class III recalls cover products not likely to cause any adverse health consequences, typically involving technical regulatory violations. The classification guides urgency, Class I recalls require immediate action, while Class III may simply involve returning a product or acknowledging a labeling change. Always read the specific recall notice for recommended patient actions.
Report problems with medical devices to the FDA through MedWatch at 1-800-FDA-1088 or online at FDA.gov/safety/medwatch. Healthcare facilities are required by law to report device-related serious injuries and deaths. Patients and consumers can also report voluntarily. Include the device name, manufacturer, model number, and a description of the problem and any patient outcome. Reports from patients and clinicians help the FDA identify emerging safety signals and may trigger investigations that lead to recalls of dangerous devices.
What Should You Do?
Stop using this device if you are affected by this recall. Contact your healthcare provider and the manufacturer immediately for guidance. Report adverse events to FDA MedWatch.