Maxi Twin KTBB4BSU2WWRecalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 05055982793360), received between Nov 2, 2020 and Nov 29, 2024 — classified as 3 injuries, 2 malfunctions.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (4 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 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• InjuryNov 29, 2024Detachment of Device or Device Component; Detachment of Device or Device Component

  THE CUSTOMER REPORTED THAT DURING RESIDENT TRANSFER THE LEFT LEG SLING CLIP DETACHED. AS A CONSEQUENCE OF THE EVENT THE RESIDENT FELL OUT FROM THE DEVICE. THE RESIDENT SUSTAINED FRACTURE TO THE SKULL AND BRAIN BLEED,

  Patient problems: Head Injury

  MAUDE report 20809491 ↗
• MalfunctionJul 22, 2024Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THAT THE RESIDENT WAS TRANSFERRED FROM A WHEELCHAIR TO A BED. WHEN THE RESIDENT WAS LIFTED FROM THE WHEELCHAIR THE SLING LEG CLIP DETACHED. THE RESIDENT SUSTAINED A BRUISING.

  Patient problems: Bruise/Contusion

  MAUDE report 19791940 ↗
• MalfunctionDec 21, 2023Device Tipped Over; Device Tipped Over

  FOLLOWING THE INFORMATION REPORTED, THE MAXI MOVE PASSIVE FLOOR LIFT TIPPED OVER. A CERTIFIED NURSING ASSISTANT (CNA) SUSTAINED THE LEFT SHOULDER STRAIN WHILE STOPPING THE LIFT FROM HURTING THE RESIDENT. X-RAYS WERE TAKEN AND NO FRACTURE WAS NOTICED. NO MAGNETIC RESONANCE IMAGING (MRI) WAS NEEDED. CNA WAS RELEASED FROM THE HOSPITAL. ALTHOUGH IT WAS CLAIMED BY THE CUSTOMER THAT THE FLOOR LIFT LEGS WOULD NOT OPEN, SUCH ISSUE WAS NOT FOUND DURING THE DEVICE INSPECTION.

  Patient problems: Muscle/Tendon Damage

  MAUDE report 18370603 ↗
• InjuryNov 2, 2020Detachment of Device or Device Component; Detachment of Device or Device Component

  ARJO WAS MADE AWARE ABOUT AN EVENT INVOLVING ARJO MAXI TWIN PASSIVE FLOOR LIFT AND CLIP SLING. IT WAS STATED THAT WHEN REMOVING THE PATIENT FROM THE BATH, JUST ABOVE THE CHAIR, THE RESIDENT MADE A SUDDEN MOVE AND A LEFT LEG CLIP DETACHED FROM THE SPREADER BAR ATTACHMENT POINT. AS THE CONSEQUENCE OF THE EVENT THE PATIENT SLIPPED OUT OF THE SLING. THE PATIENT SUSTAINED A DEEP CUT ON THE LEG REQUIRING STITCHES (CALF AREA), ABRASIONS AND BUMP ON THE HEAD (CAT SCAN WAS NEEDED).

  Patient problems: Abrasion; Fall; Head Injury; Skin Tears

  MAUDE report 10768757 ↗
• InjuryNov 2, 2020Detachment of Device or Device Component; Detachment of Device or Device Component

  ARJO WAS MADE AWARE ABOUT AN EVENT INVOLVING ARJO MAXI TWIN PASSIVE FLOOR LIFT AND CLIP SLING. IT WAS STATED THAT WHEN REMOVING THE PATIENT FROM THE BATH, JUST ABOVE THE CHAIR, THE RESIDENT MADE A SUDDEN MOVE AND A LEFT LEG CLIP DETACHED FROM THE SPREADER BAR ATTACHMENT POINT. AS THE CONSEQUENCE OF THE EVENT THE PATIENT SLIPPED OUT OF THE SLING. THE PATIENT SUSTAINED A DEEP CUT ON THE LEG REQUIRING STITCHES (CALF AREA), ABRASIONS AND BUMP ON THE HEAD (CAT SCAN WAS NEEDED).

  Patient problems: Abrasion; Fall; Head Injury; Skin Tears

  MAUDE report 10768755 ↗