Arjo Sling MFA1000M-XLRecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 05055982770897), received between Jun 9, 2022 and Aug 13, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Break” (2 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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 13, 2026Break; Detachment of Device or Device Component

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50231533 ↗
• MalfunctionAug 25, 2025Break; Break

  A PATIENT FELL ONTO THEIR BED AFTER THE SLING BROKE DURING TRANSFER. THE SLING WAS DISCARDED BY STAFF AFTER THE INCIDENT. NO INJURY WAS REPORTED.

  Patient problems: Fall; No Clinical Signs, Symptoms or Conditions

  MAUDE report 22882790 ↗
• MalfunctionJun 9, 2022Material Rupture; Material Rupture

  THE MANAGER ON M-6 BOB REPORTED THAT THE ARJO SLING LOOP RIPPED OFF WHEN THEY WERE TRANSFERRING A PT BACK TO BED. THE PT IS WAY UNDER THE SLINGS WEIGHT LIMIT.. FORTUNATELY THE PATIENT WAS OVER THE BED WITH NO INJURY ORIGINAL SHORT DESCRIPTION: ADVERSE EVENT / NEAR MISS IT WAS REPORTED THAT PATIENT WAS TRANSFER FROM A RECLINER TO THE BED. WHILE THE PATIENT WAS OVER THE BED, PART OF THE SLING MATERIAL SUDDENLY RIPPED AND SLING PARTIALLY DETACHED FROM A LIFT. THE STAFF WAS ABLE TO SUPPORT THE PATIENT AND NO INJURY WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14641546 ↗