Arjo Sling AHD001Recalls & reported problems
Arjohuntleigh AB · Disposable loop repositioning sling · Class 1
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 05055982793537), received between Jun 24, 2021 and Jun 25, 2021 — classified as 3 injuries.
The most frequently reported specific device problem is “Material Deformation” (3 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
Device problems
- Material Deformation3
- Use of Device Problem3
Patient problems
- Bruise/Contusion1
- Laceration(s)1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryJun 25, 2021Use of Device Problem; Material Deformation; Use of Device Problem; Material Deformation
ARJO WAS NOTIFIED ABOUT EVENTS REGARDING DISPOSABLE REPOSITIONING SLING. THE CUSTOMER REPORTED THAT TWO EVENTS OCCURRED. BOTH WERE REPORTED UNDER MEDWATCH REPORTS NUMBERS 3012292104-2021-00013.
Patient problems: Bruise/Contusion
MAUDE report 12064852 ↗InjuryJun 24, 2021Use of Device Problem; Material Deformation; Use of Device Problem; Material Deformation
ARJO WAS NOTIFIED ABOUT EVENTS REGARDING DISPOSABLE REPOSITIONING SLING. THE CUSTOMER REPORTED THAT TWO EVENTS OCCURRED. BOTH WERE REPORTED UNDER MEDWATCH REPORTS NUMBERS 3012292104-2021-00014. THE INVESTIGATION CONCERN THE FIRST COMPLAINT. IT WAS REPORTED THAT A CAREGIVER WAS PERFORMING PATIENT CARE. WHEN THE CAREGIVER TURNED AROUND TO SWITCH OFF THE DEVICE WHICH STARTED TO ALARMING, SHE DID NOT NOTICE THAT HER FOOT WAS CAUGHT BY A SLING LOOP THAT WAS HANGING ON THE FLOOR. AS A CONSEQUENCE OF THE EVENT THE CAREGIVER FELL AND SUSTAINED WRENCHED HER BACK AND RIGHT HIP.
Patient problems: Laceration(s)
MAUDE report 12056636 ↗InjuryJun 24, 2021Use of Device Problem; Material Deformation; Use of Device Problem; Material Deformation
ARJO WAS NOTIFIED ABOUT EVENTS REGARDING DISPOSABLE REPOSITIONING SLING. THE CUSTOMER REPORTED THAT TWO EVENTS OCCURRED. BOTH WERE REPORTED UNDER MEDWATCH REPORTS NUMBERS 3012292104-2021-00012. THE INVESTIGATION CONCERN FIRST COMPLAINT. IT WAS REPORTED THAT EMPLOYEE WAS PERFORMING PATIENT CARE WHEN TRIPPED OVER THE SLING LOOPS THAT WAS HANGING ON THE FLOOR . AS A CONSEQUENCE OF THE EVENT THE CAREGIVER FELL. NO INJURY WAS SUSTAINED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12056424 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.