SmartBand SafeGrip Multi-Band Ligation Kit SLK6LFRecalls & reported problems
US Endoscopy · Multi-Band Ligation Kit · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00724995247331), received between Jan 28, 2026 and Jul 27, 2026 — classified as 1 injury, 2 malfunctions.
The most frequently reported specific device problem is “Failure to Advance” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Failure to Advance1
- Insufficient Device Problem Information1
- Unintended Movement1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryJul 27, 2026Failure to Advance
The user facility reported that during a patient procedure, multiple attempts were made to deploy the SmartBand SafeGrip Multi-Band Ligation Kit following successful tissue capture. The procedure was completed successfully; however, a procedural delay was reported as the facility had to use another device before continuing the procedure.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50006441 ↗MalfunctionJun 16, 2026Unintended Movement
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE TWO OF THE ELASTIC BANDS TO THEIR SMARTBAND MULTI-BAND LITIGATION KIT RELEASED AT THE SAME TIME AND ONE OF THEM BECAME STUCK AT THE GASTROINTESTINAL JUNCTION. THE PROCEDURE WAS COMPLETED SUCCESSFULLY FOLLOWING A SHORT DELAY TO LOCATE THE ELASTIC BAND. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25521941 ↗MalfunctionJan 28, 2026Insufficient Device Problem Information
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE, THE CORD THAT DEPLOYS BANDS THROUGH THEIR SMARTBAND SAFEGRIP MULTI-BAND LIGATION KIT BROKE. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24203601 ↗
Other Ligator, hemorrhoidal devices
- ShortShot G34063Cook Ireland Ltd · Ligator, hemorrhoidal31 reports
- SmartBand SafeGrip Multi-Band Ligation Kit SLK-6-LFIntelligent Endoscopy LLC · Ligator, hemorrhoidal9 reports
- SmartBand Ligation Kit SLK-6Intelligent Endoscopy LLC · Ligator, hemorrhoidal1 report
- SPACEBANDER HB1020Conmed Corporation · Ligator, hemorrhoidal1 report
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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