Multirall™ overhead lift 3130001Recalls & reported problems

Summary

The FDA's MAUDE database contains 25 adverse event reports that list this exact device (DI 00887761982284), received between Dec 7, 2023 and Jun 1, 2026 — classified as 5 injuries, 20 malfunctions.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (8 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 25 most recent of 25 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 1, 2026Failure to Auto Stop

  BAXTER RECEIVED A REPORT THAT MULTIRALL 200 HAD EMERGENCY STOP BUTTON INOPERATIVE. 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 25356113 ↗
• MalfunctionMay 15, 2026Detachment of Device or Device Component

  BAXTER RECEIVED A REPORT THAT MULTIRALL 200 HAD STRAP FALLING ON PATIENT. THIS OCCURRED DURING PATIENT USE. IT WAS REPORTED THAT THERE WAS NOT PATIENT/USER INJURY OR MEDICAL INTERVENTION WITH THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25192445 ↗
• MalfunctionMay 7, 2026Device Fell

  BAXTER RECEIVED A REPORT THAT MULTIRALL HAD ENGINE FALL. THE STRAP DETACHED FROM THE RAIL WITHOUT THE PATIENT PRESENT, MEDICAL STAFF INTERVENED TO SECURE THE MOTOR MID-AIR, BUT THE ATTACHMENT SUBSEQUENTLY FELL ONTO THE PATIENT. THE PROCESS STEP DURING WHICH THIS OCCURRED WAS DURING USE. THERE WAS NOT PATIENT INJURY.

  Patient problems: Hematoma

  MAUDE report 25117340 ↗
• InjuryApr 24, 2026Misconnection; Device Fell

  IT WAS REPORTED THAT A PATIENT FELL FROM A MULTIRALL 200 LIFT AND SUSTAINED MULTIPLE FRACTURES. DURING PATIENT TRANSFER, THE PATIENT FELL FROM THE LIFT, APPROXIMATELY 1.5 METERS. AFTER AN INSPECTION BY BAXTER IT WAS NOTED THAT AT THE TIME OF THE INCIDENT THE LIFT WAS EQUIPPED WITH A QLINK INSTEAD OF A QLINK II, AS THE CUSTOMER¿S BIOMEDICAL DEPARTMENT HAD REPLACED IT WITH AN OLD MODEL, DESPITE BAXTER RECOMMENDATIONS. THE REPORTED FRACTURES ARE AWAITING CONFIRMATION VIA CT SCAN, AND THE PATIENT REQUIRED A PROLONGED HOSPITALIZATION. THE EXACT CAUSE IS UNDETERMINED AT THIS TIME; HOWEVER, A USE ERROR CANNOT BE EXCLUDED AS THE LIFT WAS BEING USED WITH AN OBSOLETE COMBINATION DESPITE BAXTER RECOMMENDATIONS. NO FURTHER INFORMATION IS AVAILABLE AT THIS TIME.

  Patient problems: Multiple Fractures

  MAUDE report 24990010 ↗
• MalfunctionApr 23, 2026Material Split, Cut or Torn

  BAXTER RECEIVED A REPORT THAT MULTIRALL 200 HAD STRAP JAMMED INSIDE THE UNIT WHEN TRYING TO REWIND IT. WHEN PRESSING THE BUTTON THE STRAP FAILED TO RETRACT AND DISCOVERED IT WAS ALL SHREDDED. 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 24973581 ↗
• InjuryMar 23, 2026Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information

  BAXTER RECIEVED A REPORT WHEN A CAREGIVER PUSHED THE LIFT TO REMOVE IT FROM THEIR WORKING AREA BUT PUSHED IT TOO HARD AND MADE IT SWING, AND WHEN IT CAME BACK, IT HIT THEM IN THE TEMPLE. THE CAREGIVER WAS ADMITTED TO THE EMERGENCY DEPARTMENT FOR A SUSPECTED HEAD INJURY AND WAS GIVEN A ONE-WEEK MEDICAL LEAVE. ADDITIONALLY, NO INITIAL DEVICE MALFUNCTION WAS REPORTED. NO FURTHER INFORMATION WAS AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Head Injury

  MAUDE report 24665109 ↗
• MalfunctionMar 13, 2026Detachment of Device or Device Component

  ON (B)(6) HAD A MOBILE LIFT MOTOR STRAP SUDDENLY UNSPOOLED, CAUSING A RESIDENT FALL. THE PROCESS STEP DURING WHICH THIS OCCURRED WAS UNKNOWN. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: Abrasion; Erythema; Laceration(s)

  MAUDE report 24595660 ↗
• MalfunctionJan 12, 2026Detachment of Device or Device Component

  A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT MULTIRALL 200 HAD AN ISSUE, DURING THE PATIENT'S TRANSFER FROM THE CHAIR TO THE BED, THE MOTOR DETACHED FROM THE RAIL. THE CAREGIVER WAS ABLE TO PUSH THE PATIENT BACK ONTO THE BED. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THE DEVICE WAS REQUESTED FOR SERVICE/INSPECTION BY BAXTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24038352 ↗
• InjuryDec 23, 2025Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED A CAREGIVER SUSTAINED AN INJURY WHEN TRANSFERRING A PATIENT IN A MULTIRALL OVERHEAD LIFT. AFTER THE CAREGIVER HAD PROVIDED NURSING CARE TO A RESIDENT, THE CAREGIVER WANTED TO TRANSFER ANOTHER RESIDENT; HOWEVER, THE MOBILE PATIENT LIFT WASN'T WORKING BECAUSE THE BATTERY WASN'T PROPERLY SECURED. INSTEAD OF USING THE OTHER MOBILE PATIENT LIFT, THE CAREGIVER TOOK THE LIFT FROM THE ROOM ACROSS THE HALL, AND SINCE THE RAIL HEIGHTS WERE DIFFERENT, THE STRAP WAS SHORT, MAKING IT DIFFICULT TO ATTACH THE LIFTING ROD. THIS RESULTED IN THE DETACHMENT OF THE LIFT. THE CAREGIVER WAS ABLE TO SAVE THE RESIDENT WHO WAS ALREADY IN THE TRANSFER NET. THE PATIENT WAS NOT HARMED; HOWEVER, IT WAS NOTED THAT THE CAREGIVER REQUIRED SICK LEAVE DUE TO CERVICAL, SHOULDER, BACK, AND LEFT ARM INJURY. NO FURTHER INFORMATION WAS AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 23881582 ↗
• MalfunctionNov 26, 2025Mechanical Problem; Key or Button Unresponsive/not Working; Mechanical Problem; Key or Button Unresponsive/not Working

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT MULTIRALL 200 (PRODUCT CODE 3130001, SERIAL NUMBER (B)(6), HAD EMERGENCY STOP BUTTON INOPERATIVE. 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 23662817 ↗
• MalfunctionNov 5, 2025Mechanical Problem; Mechanical Problem

  A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT MULTIRALL 200 HAD AN ISSUE AND NEEDED REPAIR. DURING INSPECTION, THE BAXTER TECHNICIAN FOUND THE EMERGENCY STOP BUTTON WAS FAULTY. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23475953 ↗
• MalfunctionSep 30, 2025Material Split, Cut or Torn; Material Split, Cut or Torn

  ANOTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT THE MULTIRALL 200 ENGINE COULD NOT BE CHARGED. PROCESS STEP DURING WHICH THIS OCCURRED WAS UNKNOWN. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. IT WAS UNKNOWN IF ANY SECOND DEVICE WAS ALSO INVOLVED. THE CUSTOMER DID NOT KNOW IF THIS EVENT WAS ALREADY COMMUNICATED TO ANOTHER BAXTER DEPARTMENT OR AUTHORITY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23180844 ↗
• MalfunctionAug 19, 2025Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THAT DURING THE USE OF THE MULTIRALL 200, THE EXTENSION BELT CAME UNDONE, AND THE ENGINE FELL ON THE PATIENTS¿ ABDOMEN. NO INJURY OR MEDICAL INTERVENTION WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22837658 ↗
• MalfunctionAug 1, 2025Mechanical Problem; Mechanical Problem

  A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT MULTIRALL 200 HAD AN ISSUE, BROKEN EMERGENCY STOP, RANDOM MALFUNCTION. THIS OCCURRED AFTER PATIENT USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED. THE CUSTOMER DID NOT COMMUNICATE THIS EVENT TO ANOTHER BAXTER DEPARTMENT OR AUTHORITY. THE DEVICE WAS REQUESTED FOR SERVICE/INSPECTION BY BAXTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22687182 ↗
• MalfunctionJul 2, 2025Mechanical Problem; Mechanical Problem

  A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT THE MULTIRALL 200 HAD AN ISSUE, UPON INSPECTION, THE BAXTER TECHNICIAN FOUND THE EMERGENCY STOP BUTTON WAS NOT FUNCTIONAL ON THE DEVICE. THE PROCESS STEP DURING WHICH THIS OCCURRED WAS UNKNOWN. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. IT WAS UNKNOWN IF ANY SECOND DEVICE WAS ALSO INVOLVED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22381946 ↗
• MalfunctionApr 4, 2025Device Fell; Device Fell

  A USER REPORT WAS RECEIVED FROM THE MPA STATING THAT THE MULTIRALL 200 LIFT HAD AN ISSUE. WHEN MOUNTING THE LIFT UP, THE LIFT RELEASED THE BLACK RIBBON. THE LIFT FELL ONTO THE PATIENT'S BED. FORTUNATELY, THE PATIENT WAS LYING TO THE RIGHT AND THE LIFT ENDED UP ON THE LEFT SIDE. 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: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21771404 ↗
• MalfunctionMar 27, 2025Detachment of Device or Device Component; Detachment of Device or Device Component

  A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT THE MULTIRALL 200 LIFT FELL. 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 21707770 ↗
• InjuryMar 19, 2025Disconnection; Disconnection

  IT WAS REPORTED A PATIENT SUSTAINED A LACERATION ABOVE THE RIGHT EYE WHEN USING A MULTIRALL OVERHEAD LIFT. DURING A PATIENT TRANSFER FROM THE BED TO A CHAIR, THE MULTIRALL 200 LIFT DETACHED FROM THE S65 HOOK, AND FELL ONTO THE PATIENT'S HEAD WHILE THEY WERE SITTING IN THE CHAIR. THE EVENT RESULTED IN A LACERATION ABOVE THE RIGHT EYE, WHICH RESULTED IN TWO STITCHES. THE PATIENT ALSO SUSTAINED A ¿POTENTIAL NASAL FRACTURE¿; HOWEVER, THERE IS NO FURTHER INFORMATION TO CONFIRM IF THERE WAS A FRACTURE. NO FURTHER INFORMATION WAS AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Laceration(s)

  MAUDE report 21648586 ↗
• MalfunctionFeb 18, 2025Material Split, Cut or Torn; Material Split, Cut or Torn

  A DISTRIBUTOR CONTACTED TECHNICAL SERVICE TO REPORT THAT MULTIRALL 200 HAD AN ISSUE, THE LIFT STRAP TORE. 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 21405301 ↗
• MalfunctionJan 9, 2025Detachment of Device or Device Component; Detachment of Device or Device Component

  A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT THE MULTIRALL 200 HAD AN ISSUE, THE EMERGENCY STOP SWITCH WAS FAULTY. THIS OCCURRED AFTER PATIENT USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED. THE DEVICE WAS REQUESTED FOR SERVICE/INSPECTION BY BAXTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21110680 ↗
• MalfunctionNov 19, 2024Component Incompatible; Component Incompatible

  A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT MULTIRALL 200 UNIT HAD A RECALL A FEW YEARS PRIOR AND THE CUSTOMER WAS NOT INFORMED BY THE 3RD PARTY THEY BOUGHT THE UNIT FROM NOR HAD THE CORRECTIVE ACTION PARTS BEEN REPLACED. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20726157 ↗
• MalfunctionOct 23, 2024Detachment of Device or Device Component; Detachment of Device or Device Component

  THE CUSTOMER ALLEGED THE LIFT¿S EMERGENCY BUTTON WAS OUT OF ORDER. THERE WAS NO ALLEGATION OF PATIENT OR CAREGIVER INJURY OR DEATH REPORTED FROM THIS ALLEGED INCIDENT. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20514120 ↗
• MalfunctionJul 16, 2024Break; Mechanical Problem; Break; Mechanical Problem

  THE CUSTOMER ALLEGED THE LIFT HAD BENT RODS ON THE INTERNAL MOTOR, CAUSING THE MOTOR TO TIGHTEN AND THE FUSE TO BE BLOWN. THERE WAS NO ALLEGATION OF PATIENT OR CAREGIVER INJURY OR DEATH REPORTED FROM THIS ALLEGED INCIDENT. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19748881 ↗
• MalfunctionDec 19, 2023Break; Break

  THE CUSTOMER ALLEGED THE SLINGBAR WAS BROKEN NEAR THE SUPPORT HOOK AND NEEDED TO BE REPLACED. THERE WAS NO ALLEGATION OF PATIENT OR CAREGIVER INJURY OR DEATH REPORTED FROM THIS ALLEGED INCIDENT. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18354896 ↗
• InjuryDec 7, 2023Device Fell; Device Fell

  THE CUSTOMER REPORTED THAT ON THE 1ST OF NOVEMBER 2023, A MULTIRALL LIFT FELL ON THE NURSE'S SHOULDER, AND THE NURSE WAS TAKEN TO THE EMERGENCY DEPARTMENT. ON THE 22ND OF NOVEMBER 2023, DURING FOLLOW-UP WITH THE HOSPITAL'S BIOMEDICAL, IT WAS REPORTED THAT THE NURSE SUFFERED OF A DOUBLE CLAVICLE (COLLARBONE) FRACTURE. SHE IS CURRENTLY IN SICK LEAVE AND WASN'T CURRENTLY ABLE TO PROVIDE INFORMATION ON THE MEDICAL TREATMENT SHE HAS / WILL RECEIVE. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS (B)(4).

  Patient problems: Bone Fracture(s)

  MAUDE report 18283158 ↗