Liko™ M230 mobile lift 2050015Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00887761981904), received between May 6, 2021 and Apr 22, 2026 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Device Fell” (2 reports).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 22, 2026Device Fell

  BAXTER RECEIVED A REPORT THAT LIKO M230 HAD A PATIENT FALLING FROM THE LIFT DURING TRANSFER. THIS OCCURRED DURING PATIENT USE. IT WAS REPORTED THAT THERE WAS NO PATIENT/USER INJURY OR MEDICAL INTERVENTION WITH THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24958092 ↗
• MalfunctionJan 23, 2026Device Fell

  ON 30-DEC-2025, A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT LIKO M230 (PRODUCT CODE 2050015, SERIAL NUMBER (B)(6)), HAD PATIENT BEING TRANSFERRED FROM A WHEELCHAIR TO A BED USING A PERSONAL LIFT WHEN THE BATTERY RAN OUT AND MADE PATIENT FALL ONTO THE BED. THIS OCCURRED DURING PATIENT USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED.

  Patient problems: Fall

  MAUDE report 24168396 ↗
• MalfunctionJan 6, 2025Mechanical Problem; Mechanical Problem

  A DISTRIBUTOR CONTACTED TECHNICAL SERVICE TO REPORT THAT LIKO M230 EMERGENCY STOP BUTTON WAS FAULTY AND NEEDED TO BE REPLACED.. THE PROCESS STEP DURING WHICH THIS OCCURRED WAS UNKNOWN. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21078428 ↗
• MalfunctionMay 6, 2021Break; Break

  HILLROM RECEIVED A REPORT FROM THE ACCOUNT STATING THE SLINGBAR HAD BROKEN LOOSE FROM THE PIVOT ATTACHMENT. THE LIFT WAS LOCATED AT THE ACCOUNT. THERE WAS A PATIENT ON THE LIFT AND WHEN THE LIFT DROPPED TO THE FLOOR, THE PATIENT DID AS WELL. THE CUSTOMER REPORTED THAT DURING USE OF THE LIKO LIFT, THE SLING BAR BROKE LOOSE FROM THE PIVOT, THE PATIENT WAS OVER THE BED AND FELL TO THE BED, AND THE SLING BAR STRUCK THE PATIENT ON THE BACK OF HER HANDS CAUSING BRUISING TO THE BACK OF HER HANDS. NO HOSPITAL TREATMENT WAS PROVIDED TO THE PATIENT, THE PATIENT WAS EVALUATED AND REPORTED TO BE OK. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT (B)(4).

  Patient problems: Fall

  MAUDE report 11785782 ↗