Maxi Twin KTBB4BSX2WWRecalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 05055982787154), received between Jun 15, 2022 and Nov 4, 2025 — classified as 2 injuries, 2 malfunctions.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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 16, 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.

• MalfunctionNov 4, 2025Unintended Movement; Unintended Movement

  THE INCIDENT OCCURRED IN A PRIVATE HOME DURING AN ATTEMPTED PATIENT TRANSFER USING A MAXI TWIN PASSIVE FLOOR LIFT. WHILE CARERS WERE RAISING THE PATIENT FROM A CHAIR TO A BED, THE LIFT ALLEGEDLY COLLAPSED. THE PATIENT WAS SAFELY RETURNED TO THE CHAIR, AND NO INJURIES WERE REPORTED. FOLLOWING THE EVENT, FIVE INDIVIDUALS ASSISTED IN FACILITATING THE PATIENT¿S TRANSFER BACK TO THE BED. THE PATIENT¿S WIFE CONTACTED A THIRD-PARTY SERVICE PROVIDER RESPONSIBLE FOR MAINTAINING THE LIFT TO ARRANGE INSPECTION AND REPAIR. THEN, THE LIFT WAS RETURNED TO THE ARJO SERVICE CENTER FOR INSPECTION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23461400 ↗
• InjuryMar 5, 2024Detachment of Device or Device Component; Detachment of Device or Device Component

  THE PATIENT WAS TRANSFER WITH MAXI TWIN PASSIVE FLOOR LIFT AND SLING (MAA4000M-XXL, SERIAL NUMBER (B)(6)). DURING THE TRANSFER THE SLING LEFT CLIP DETACHED AND PATIENT FELL OUT OF THE DEVICE. THE CAREGIVERS WERE LIFTED ONE THIGH OF THE PATIENT WHEN POSITIONING ABOVE THE BED AT THE TIME WHEN THE EVENT OCCURED. HEAD INJURY CONFIRMED AND HOSPITALIZATION OF THE PATIENT AFTER THE EVENT.

  Patient problems: Head Injury

  MAUDE report 18834848 ↗
• InjuryMar 5, 2024Detachment of Device or Device Component; Detachment of Device or Device Component

  THE PATIENT WAS TRANSFER WITH MAXI TWIN PASSIVE FLOOR LIFT AND SLING (MAA4000M-XXL, SERIAL NUMBER (B)(6)). DURING THE TRANSFER THE SLING LEFT CLIP DETACHED AND PATIENT FELL OUT OF THE DEVICE. THE CAREGIVERS WERE LIFTED ONE THIGH OF THE PATIENT WHEN POSITIONING ABOVE THE BED AT THE TIME WHEN THE EVENT OCCURED. HEAD INJURY CONFIRMED AND HOSPITALIZATION OF THE PATIENT AFTER THE EVENT.

  Patient problems: Fall; Head Injury

  MAUDE report 18834847 ↗
• MalfunctionJun 15, 2022Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THAT DURING PATIENT TRANSFER, TWO CAREGIVERS LIFT PATIENT FROM THE BED AND THE LEG SLING DETACHED. THE PATIENT FELL OUT OF BED. NO INJURY WAS SUSTAINED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14692387 ↗