Golvo mobile liftRecalls & reported problems across all models
Liko AB · 3 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 47
- Deaths reported
- 0
- Injuries reported
- 7
- Recalls
- 0
We found 3 models of Golvo mobile lift by Liko AB in the FDA's device registry (GUDID). Together they are named in 47 adverse event reports in the FDA's MAUDE database, received between May 25, 2022 and Sep 23, 2026 — classified as 7 injuries, 40 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (23 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported Golvo mobile lift problems
Device problems
- Detachment of Device or Device Component23
- Material Split, Cut or Torn5
- Device Fell4
- Adverse Event Without Identified Device or Use Problem3
- Device Tipped Over2
- Insufficient Device Problem Information2
- Mechanical Problem2
- Unstable2
Patient problems
- No Clinical Signs, Symptoms or Conditions38
- Fall2
- Head Injury2
- Hematoma2
- Laceration(s)2
- Back pain1
- Hemorrhage/Blood Loss/Bleeding1
- Hip Fracture1
Golvo mobile lift models
3 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Golvo™ mobile lift 2000049Lift, patient, non-ac-powered28 reports
- Golvo™ mobile lift 2000045Lift, patient, non-ac-powered17 reports
- Golvo™ mobile lift 2000049CNLift, patient, non-ac-powered2 reports
Recent Golvo mobile lift adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 23, 2026Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50875586 ↗MalfunctionSep 1, 2026Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50551515 ↗MalfunctionAug 13, 2026Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50244472 ↗MalfunctionAug 11, 2026Sparking
Baxter received a report that GOLVO 9000 had power cable and control box burnt. There was no patient/user injury, medical intervention, symptom, or adverse event reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50212269 ↗MalfunctionJul 14, 2026Device Fell
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25820859 ↗MalfunctionJun 29, 2026Device Fell
BAXTER RECEIVED A REPORT THAT A GOLVO 7000 ES HAD DEVICE FALLING. THIS OCCURRED DURING PATIENT USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25660992 ↗MalfunctionJun 22, 2026Flare or Flash
BAXTER RECEIVED A REPORT THAT GOLVO 8008 LOWBASE HAD POWER CORD COMING OUT OF WALL INTO PIGTAIL MELTED / STATED ELECTRICAL FIRE OCCURRED. THIS OCCURRED AFTER PATIENT USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25588324 ↗MalfunctionJun 9, 2026Detachment of Device or Device Component
BAXTER RECEIVED A REPORT THAT GOLVO 9000 LOWBASE HAD FRONT RIGHT CASTER FALLEN OFF. THIS OCCURRED BEFORE USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25449578 ↗MalfunctionJun 3, 2026Detachment of Device or Device Component
BAXTER RECEIVED A REPORT THAT GOLVO 9000 HAD WHEELS COMING OFF THE LIFT. 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 25383761 ↗MalfunctionMay 15, 2026Material Split, Cut or Torn
BAXTER RECEIVED A REPORT THAT GOLVO 8008 WITH CABLE HAD POWER CABLE DAMAGED WITH COPPER WIRES EXPOSED. THIS OCCURRED DURING BAXTER SERVICING/TESTING. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25190797 ↗MalfunctionMay 14, 2026Detachment of Device or Device Component
IT WAS REPORTED A PATIENT FELL FROM A GOLVO MOBILE LIFT DURING A TRANSFER. DURING THE PATIENT TRANSFER, THE PATIENT SHIFTED, CAUSING THE SLING BAR TO TILT, A LATCH TO SNAP OFF, AND THE SLING TO SLIDE OFF THE HOOK. THE PATIENT WAS TRANSFERRED TO THE EMERGENCY DEPARTMENT (ED) FOR EVALUATION AND WAS DISCHARGED WITH NO INJURIES. A DEVICE INSPECTION PERFORMED BY A BAXTER TECHNICIAN NOTED THAT THE LIFT WAS WORKING AS DESIGNED AND THE BATTERY WAS REPLACED. THE SLING USED WAS NOTED TO BE FROM AN UNKNOWN MANUFACTURER, AND THE EVENT WAS LIKELY DUE TO EXCESSIVE PATIENT MOVEMENT CAUSING THE SYSTEM TO BECOME UNBALANCED. THE GOLVO 9000 INSTRUCTION FOR USE (IFU) STATES: "ENSURE THAT THE LIFTING ACCESSORIES ARE SUITABLE FOR THE LIFT USED. EXERCISE CARE AND CAUTION DURING USE. AS A CAREGIVER, YOU ARE ALWAYS RESPONSIBLE FOR THE PATIENT¿S SAFETY. NO FURTHER INFORMATION WAS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Fall
MAUDE report 25167125 ↗MalfunctionApr 6, 2026Use of Device Problem; Detachment of Device or Device Component
BAXTER RECEIVED A REPORT THAT GOLVO 8008 HAD A LIFT SLING DISENGAGING FROM THE LOOP AT THE TOP RIGHT CORNER. THIS OCCURRED DURING PATIENT USE. THERE WAS NO PATIENT/USER INJURY OR MEDICAL INTERVENTION WITH THIS EVENT.
Patient problems: Hematoma; No Clinical Signs, Symptoms or Conditions
MAUDE report 24793562 ↗MalfunctionApr 6, 2026Material Split, Cut or Torn
BAXTER RECEIVED A REPORT THAT GOLVO 7007 ES HAD POWER CORD DAMAGED WITH COPPER WIRE EXPOSED. 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 24793023 ↗MalfunctionApr 2, 2026Detachment of Device or Device Component
BAXTER RECEIVED A REPORT THAT GOLVO 9000 LOWBASE HAD A FALLEN FRONT WHEEL. 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 24772237 ↗MalfunctionMar 23, 2026Unstable
ON 26-FEB-2026, A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT GOLVO 7007 LOWBASE (PRODUCT CODE P2000061, SERIAL NUMBER (B)(6), LEG IS BENT. 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 24670461 ↗
Other Liko AB products
All Liko AB devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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