Uno™ mobile lift 2010004Recalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 00887761981775), received between Nov 5, 2024 and Sep 11, 2026 — classified as 2 injuries, 5 malfunctions.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (2 reports).

1 FDA recall record name this device's identifier, 1 still open.

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.

Recalls naming this device

1. May 30, 2025Open, Classified

   The Q-link 13 could allow for an improper attachment (false latching) of the Quick-Release Hook used on Sling Bars and other accessories. This could result in a critical injury from a patient fall as the false latched component may initially bear weight but can loosen from the Q-link resulting in a detachment and drop.

   Z-2031-2025 · Root cause: Device Design · FDA record ↗

Most reported problems

Recent adverse event reports

The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 11, 2026Unstable

  Baxter received a report that UNO 102 EE had joint of the lift arm with the vertical post becoming loose. The lift was stationary. There was no patient/user injury, medical intervention, symptom, or adverse event reported.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50725305 ↗
• MalfunctionFeb 24, 2026Device Fell

  ON 29-JAN-2026, A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT UNO 102 ES (PRODUCT CODE P2010005, SERIAL NUMBER (B)(6)), HAD IMPROPERLY POSITIONED HOOK, RESULTING IN A PATIENT FALL. THE FALL WAS ESTIMATED TO BE A FEW CENTIMETERS ABOVE THE BED. 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 24431376 ↗
• InjuryDec 31, 2025Disconnection; Disconnection

  DURING THE TRANSFER OF A PATIENT TO A BED USING AN UNO MOBILE PATIENT LIFTING SYSTEM, THE HOOK (CONNECTING THE SLINGBAR TO THE LIFT ARM) CAME OFF. THE HOOK HIT THE PATIENT ON THE FOREARM AS IT DROPPED AND CAUSED THE PATIENT TO FALL A SHORT DISTANCE ON TO THE MATTRESS OF THE BED. THE PATIENT WAS NOT INJURED FROM THE FALL, HOWEVER, SUSTAINED A 15CM LACERATION TO THE FOREARM FROM THE HOOK. THE INJURY WAS CLEANED AND THEN CLOSED WITH SUTURES, AND A SLING WAS APPLIED. AN X-RAY CONFIRMED NO FRACTURE. NO ADDITIONAL INFORMATION WAS AVAILABLE.

  Patient problems: Laceration(s)

  MAUDE report 23934131 ↗
• MalfunctionApr 3, 2025Device Tipped Over; Device Tipped Over

  A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT THE UNO 102 EE LIFT HAD AN ISSUE, CUSTOMER ALLEGES THAT THE LIFT IS TIPPING TO THE RIGHT. THE PROCESS STEP DURING WHICH THIS OCCURRED WAS UNKNOWN. 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 21761069 ↗
• MalfunctionMar 10, 2025Material Twisted/Bent; Material Twisted/Bent

  A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT THE UNO 102 EE HAD AN ISSUE, THE LEFT LEG WAS BENT OFF THE FLOOR. 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 21558903 ↗
• MalfunctionJan 27, 2025Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THAT WITH DURING A TRANSFER FROM WHEELCHAIR TO BED USING AN UNO 102 LIFT AND NON-LIKO SLING (HUMAN CARE), THE SLING BAR DETACHED, AND THE PATIENT FELL FIRST ONTO THE BED, AND THEN ONTO THE FLOOR. THE PATIENT REPORTED PAIN AFTER THE FALL, AND A RED MARK WAS OBSERVED ON THEIR BACK. NO MEDICAL INTERVENTION WAS REQUIRED. THE STAFF INVOLVED IN THE EVENT DID NOT REPORT ANY SING OF DEVICE MALFUNCTION.

  Patient problems: Pain

  MAUDE report 21241289 ↗
• InjuryNov 5, 2024Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THAT AS A PATIENT WAS BEING TRANSFERRED FROM HIS BED TO A WHEELCHAIR USING THE UNO 102 LIFT, THE LIFT¿S ¿JUMPER¿ (SLINGBAR) DETACHED AT THE QUICK RELEASE WHILE THE PATIENT WAS HANGING IN THE LIFT. THE PATIENT FELL DOWN TO THE EDGE OF THE BED AND THEN SLID DOWN THE SIDE OF THE BED TO THE FLOOR. AS THE PATIENT SLID DOWN, HE HIT HIS HEAD ON THE EDGE OF THE BED. IT IS NOTED THAT THE PATIENT WAS ALERT AND TALKATIVE FOLLOWING THE FALL BUT WAS SUBSEQUENTLY TAKEN TO THE HOSPITAL BY AMBULANCE DUE TO ¿PAIN.¿ THE PATIENT WAS PROVIDED OXYGEN AND A CT OF THE BRAIN, CERVICAL SPINE, AND LUMBAR SPINE WAS PERFORMED WHICH FOUND A ¿SLIGHT COMPRESSION IN THE L3 VERTEBRAE, THE BRAIN AND CERVICAL SPINE WERE NOTED TO BE UNREMARKABLE. IT IS NOTED THE OXYGEN WAS ¿PHASED OUT¿ AND THE PATIENT¿S PAIN WAS TREATED WITH BUPRENORPHINE PATCH WHICH WAS LATER CHANGED TO ¿OXYNORM AND ULTIMATELY NORGESIC AND ALVEDON.¿ THE PATIENT WAS REPORTED TO HAVE FREE MOBILIZATION WHEN DISCHARGED HOME TO HIS HEALTHCARE CENTER.

  Patient problems: Pain; Vertebral Fracture

  MAUDE report 20614700 ↗