Recall Z-0151-2027 ยท FSA Lift, Patient, Non-Ac-Powered
Baxter Healthcare Corporation
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 Descripti
| Date | Oct 13, 2026 (initiated Sep 14, 2026) |
| Status | Open, Classified |
| Reason | 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. |
| Root cause | Process control |
| Action | The firm began mailing Urgent Medical Device Correction letters to facilities on September 14, 2026. Home patient communication was sent on September 15, 2026. Customers were informed that Baxter has developed procedures to inspect devices and correct them as needed. A Baxter representative will contact customer facilities to provide instructions or to coordinate onsite completion of these activities. The firm recommends that a Mobile Lift be used as an alternative until the correction can be made. Additional safety precautions were given in case the customer chooses to continue to use poten |
| 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, |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
This recall record lists no 510(k) number.