Arjo Sling MAA2040M-LLRecalls & reported problems
Arjohuntleigh AB · Clip in situ sling – unpadded legs - LL · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 05056097360126), received between Apr 7, 2022 and Apr 7, 2022 — classified as 2 injuries.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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 16, 2026.
Most reported problems
Device problems
- Detachment of Device or Device Component2
Patient problems
- Fall2
- Hip Fracture2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryApr 7, 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-LL, SERIAL NUMBER: (B)(4)) AND THE CEILING LIFT FROM THE TR-CARE COMPANY (NON-ARJO DEVICE). IT WAS REPORTED THAT WHILE TRANSFERRING THE PATIENT, THE RIGHT SHOULDER SLING CLIP BECAME LOOSE, RESULTING IN THE PATIENT FALLING TO THE FLOOR AND HITTING HER HEAD ON THE SHOWER SEAT. AS A RESULT OF THIS INCIDENT, THE PATIENT SUSTAINED A NOSEBLEED AND A HIP FRACTURE THAT REQUIRED SURGICAL INTERVENTION.
Patient problems: Fall; Hip Fracture
MAUDE report 14039639 ↗InjuryApr 7, 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-LL, SERIAL NUMBER: (B)(4)) AND THE CEILING LIFT FROM THE TR-CARE COMPANY (NON-ARJO DEVICE). IT WAS REPORTED THAT WHILE TRANSFERRING THE PATIENT, THE RIGHT SHOULDER SLING CLIP BECAME LOOSE, RESULTING IN THE PATIENT FALLING TO THE FLOOR AND HITTING HER HEAD ON THE SHOWER SEAT. AS A RESULT OF THIS INCIDENT, THE PATIENT SUSTAINED A NOSEBLEED AND A HIP FRACTURE THAT REQUIRED SURGICAL INTERVENTION.
Patient problems: Fall; Hip Fracture
MAUDE report 14039638 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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