Slings NA1004Recalls & reported problems
Joerns Healthcare, LLC · SLING,QUICKFIT NET,6-PT,MED · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00810055883455), received between Apr 29, 2025 and Apr 29, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Insufficient Device Problem 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.
Reports received per month
Most reported problems
Device problems
- Insufficient Device Problem Information1
Patient problems
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 29, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
IT WAS REPORTED TO THE MANUFACTURER, BY THE END USER, PER THE END USER, THAT CUSTOMER STATES THE QUICK FIT (STANDARD) MESH SLINGS ARE PINCHING RESIDENTS SKIN BETWEEN THEIR LEGS AND UPPER THIGH AND ARE A LOT LESS COMFORTABLE THAN THE QUICK FIT DELUXE MESH SLINGS AND CAUSING PAIN FOR RESIDENTS. DURING A TRANSFER, THE STANDARD VERSION CAUSED THE RESIDENT TO CALL OUT IN DISCOMFORT DUE TO THE PULLING (THE PROCESS WAS ENDED). WAS VERIFIED THE SLING WAS PROPERLY PLACED AND USED. THE DELUXE VERSION DID NOT PULL AND THERE WAS NO CALLING OUT. COMPLAINT #(B)(4) WAS ENTERED INTO OUR SYSTEM.
Patient problems: Pain
MAUDE report 21931897 ↗
Other Lift, Patient, Non-Ac-Powered devices
- MEDLINE MDS88200DMedline Industries, Inc. · Lift, patient, non-ac-powered108 reports
- Medline MDS600ELBMedline Industries, Inc. · Lift, patient, non-ac-powered82 reports
- Medline MDS400ELBMedline Industries, Inc. · Lift, patient, non-ac-powered79 reports
- MEDLINE MDS88200HLMedline Industries, Inc. · Lift, patient, non-ac-powered77 reports
- Viking™ XL mobile lift 2040043Liko AB · Lift, patient, non-ac-powered1 recall14 reports
- Uno™ mobile lift 2010004Liko AB · Lift, patient, non-ac-powered1 recall7 reports
- Viking™ L mobile lift 2040044Liko AB · Lift, patient, non-ac-powered1 recall4 reports
- Viking™ M mobile lift 2040045Liko AB · Lift, patient, non-ac-powered51 reports
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.
How reports and recalls are matched · Editorial policy · Report an error on this page