Arjo Sling MAA2040M-LRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05056097336855), received between Feb 25, 2022 and Feb 25, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).

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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionFeb 25, 2022Detachment of Device or Device Component; Detachment of Device or Device Component

  ARJO WAS INFORMED ABOUT AN INCIDENT INVOLVING THE ARJO PASSIVE CLIP SLING (MODEL NUMBER: MAA2040M-M-L1, SERIAL NUMBER: (B)(4)) AND THE FLOOR LIFT FROM THE TR-CARE COMPANY (NON ARJO DEVICE). IT WAS REPORTED THAT A CAREGIVER ATTEMPTED TO TRANSFER THE PATIENT WHO WAS LYING ON THE BED. THE PASSIVE CLIP SLING WAS PLACED UNDER THE PATIENT. DURING ATTACHING THE SLING TO THE LIFT, CAREGIVER NOTICED THAT THE RIGHT SHOULDER CLIP DETACHED FROM THE SPREADER BAR. THE CAREGIVER REATTACHED THE CLIP AND RAISED THE PATIENT ABOVE THE BED WHEN SUDDENLY THE LEFT SHOULDER CLIP DETACHED FROM THE SPREADER BAR. AS A CONSEQUENCE, THE PATIENT FELL DOWN ON THE BED (APPROXIMATELY 20-30 CM). THE FALL DID NOT RESULT IN ANY INJURIES.

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

  MAUDE report 13598459 ↗