Arjo Sling MFA2100-MRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05056341602385), received between Apr 27, 2023 and Apr 27, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Unclear Information” (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.

• MalfunctionApr 27, 2023Use of Device Problem; Unclear Information; Use of Device Problem; Unclear Information

  ARJO WAS INFORMED ABOUT AN EVENT INVOLVING NON-ARJO LIFT KCARE HEALTHCARE MODEL NUMBER: KH404F AND SERIAL NUMBER. : (B)(6)) AND ARJO SLING CLIP. FOLLOWING THE INFORMATION PROVIDED A PATIENT WAS TRANSFERRED FROM A CHAIR TO A BED. DURING RAISING THE LIFT WHEN THE CAREGIVER REMOVED THE CHAIR, THE PATIENT FELL THROUGH THE SLING ON THE FLOOR (DISTANCE OF APPROXIMATELY 80CM). AS A CONSEQUENCE OF THE EVENT, THE PATIENT SUSTAINED BRUISING AND A SMALL HEAD LACERATION. THE CUSTOMER DID NOT REPORT ANY MALFUNCTIONS OF THE LIFT OR SLING.

  Patient problems: Fall; Laceration(s)

  MAUDE report 16822199 ↗