Sabina™ mobile lift 2020003Recalls & reported problems

Summary

The FDA's MAUDE database contains 15 adverse event reports that list this exact device (DI 00887761981782), received between Jan 26, 2022 and Sep 29, 2026 — classified as 1 injury, 14 malfunctions.

The most frequently reported specific device problem is “Material Split, Cut or Torn” (3 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 15 most recent of 15 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 29, 2026Break

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50941343 ↗
• MalfunctionSep 8, 2026Fail-Safe Did Not Operate

  Patient problems: Discomfort

  MAUDE report 50658910 ↗
• MalfunctionJul 16, 2026Failure to Auto Stop

  BAXTER RECEIVED A REPORT THAT SABINA II EE HAD EMERGENCY STOP BUTTON INOPERATIVE. 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 25846659 ↗
• MalfunctionJun 23, 2026Failure to Auto Stop

  BAXTER RECEIVED A REPORT THAT SABINA II EE BASIC HAD MISSING EMERGENCY BUTTON ON CONTROL BOX. UNABLE TO ACTIVATE. 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 25600207 ↗
• MalfunctionApr 15, 2026Material Split, Cut or Torn

  BAXTER RECEIVED A REPORT THAT SABINA II EE BASIC HAD POWER CABLE DAMAGED WITH COPPER 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 24887559 ↗
• MalfunctionMar 20, 2026Retraction Problem

  ON 25-FEB-2026, A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT SABINA II EE (PRODUCT CODE 2020003, SERIAL NUMBER (B)(6)), EMERGENCY STOP DAMAGED, UNABLE TO ACTIVATE IT. 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 24652040 ↗
• MalfunctionMar 11, 2026Mechanical Problem

  ON 13-FEB-2026, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT SABINA II EE BASIC (PRODUCT CODE P2020003, SERIAL NUMBER (B)(6)), HAD MAST WELDMENT CRACKED. 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 24571560 ↗
• MalfunctionDec 17, 2025Mechanical Problem; Mechanical Problem

  A DISTRIBUTOR CONTACTED TECHNICAL SERVICE TO REPORT THAT THE SABINA II EE HAD AN ISSUE, THE SLINGBAR (B)(6) WAS UNUSED FROM STOCK AND OUT OF THE BOX. THE CUSTOMER NOTICED THERE WERE LOOSE SCREWS ON THE SLINGBAR. IT WAS REPORTED THE LOOSE SCREWS WERE NOT OBVIOUS BECAUSE THEY ARE ASSEMBLED TO THE BOTTOM SIDE OF TUBE. 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 23830315 ↗
• MalfunctionDec 3, 2025Detachment of Device or Device Component; Insufficient Device Problem Information; Detachment of Device or Device Component; Insufficient Device Problem Information

  A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT SABINA II EE HAD AN ISSUE, CUSTOMER REPORTED AN INCIDENT THAT OCCURRED TO A PATIENT WITH SABINA LIFT WHEN THE LIFT BROKE WHILE THE PATIENT ATTACHED TO THE LIFT, THE RESIDENT WAS LOWERED TO THE SAFETY BACK IN THE WHEELCHAIR. NO INJURY CONFIRMED, THIS OCCURRED DURING PATIENT USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23704237 ↗
• InjuryJul 2, 2025Use of Incorrect Control/Treatment Settings; Improper or Incorrect Procedure or Method; Use of Incorrect Control/Treatment Settings; Improper or Incorrect Procedure or Method

  IT WAS REPORTED A PATIENT SUFFERED A DISLOCATED SHOULDER WITH A SABINA MOBILE LIFT. REPORTEDLY, THE CAREGIVER ¿WAS NOT USING THE SLING CORRECTLY¿ AND THE PATIENT SUSTAINED A DISLOCATED SHOULDER (NO FURTHER INFORMATION ON TESTING OR MEDICAL INFORMATION WERE PROVIDED). NO FURTHER INFORMATION WAS AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Joint Dislocation

  MAUDE report 22383719 ↗
• MalfunctionMar 19, 2025Material Split, Cut or Torn; Material Split, Cut or Torn

  THE CUSTOMER REPORTED TO BAXTER THAT THE SABINA II HAD A BROKEN POWER CORD. UPON INSPECTION, THE BAXTER TECHNICIAN FOUND THE POWER CORD WAS DAMAGED WITH EXPOSED COPPER WIRES. 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.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21641224 ↗
• MalfunctionNov 13, 2024Sparking; Sparking

  A DISTRIBUTOR CONTACTED TECHNICAL SERVICE TO REPORT THAT THE SABINA II EE LIFT, SPARKS WHERE THERE IS A CONNECTION FOR THE SOCKET WHEN IT IS PLUGGED IN. 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. 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 20672680 ↗
• MalfunctionSep 12, 2024Material Split, Cut or Torn; Material Split, Cut or Torn

  THE CUSTOMER ALLEGED THE LIFT WAS NOT CHARGING CORRECTLY. THERE WAS NO ALLEGATION OF PATIENT OR CAREGIVER INJURY OR DEATH REPORTED FROM THIS ALLEGED INCIDENT. THIS INCIDENT WAS CAPTURED UNDER HILLROM COMPLAINT REF # (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20200622 ↗
• MalfunctionSep 6, 2023Material Deformation; Material Deformation

  THE CUSTOMER REPORTED THAT THE UNIT CONTROL BOX WAS DAMAGED AND LOOKED LIKE THE EMERGENCY STOP BUTTON WAS SMASHED. THERE WAS NO ALLEGATION OF PATIENT OR CAREGIVER INJURY OR DEATH REPORTED FROM THIS ALLEGED INCIDENT. THIS INCIDENT WAS CAPTURED UNDER HILLROM COMPLAINT REF # (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17694496 ↗
• MalfunctionJan 26, 2022Key or Button Unresponsive/not Working; Key or Button Unresponsive/not Working

  HILLROM RECEIVED A REPORT FROM THE ACCOUNT THAT THE EMERGENCY STOP ON THE SABINA II EE SIT TO STAND LIFT IS NOT WORKING. THERE WAS NO PATIENT/USER INJURY REPORTED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT #: (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13357821 ↗