iSnare 00711084 (UDI 00724995180782)Recalls & reported problems
US Endoscopy · The iSnare system-Lariat snare is used to inject various types of media and to grasp, dissect and transect tissue during gastrointestinal endoscopy procedures, and can be used with or without monopolar diathermic energy. · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00724995180782), received between Nov 18, 2022 and Aug 27, 2026 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Insufficient Device Problem Information2
- Retraction Problem2
- Improper or Incorrect Procedure or Method1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 27, 2026Insufficient Device Problem Information
The user facility reported that during a patient procedure, the needle to their iSnare system ¿ Lariat snare was getting stuck in the out position after injection, even when the luer lock handle was depressed. User facility personnel utilized another device, and the procedure was completed successfully. No report of injury.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50479760 ↗MalfunctionApr 3, 2025Improper or Incorrect Procedure or Method; Insufficient Device Problem Information; Improper or Incorrect Procedure or Method; Insufficient Device Problem Information
THE USER FACILITY REPORTED VIA MEDWATCH (B)(4) THAT THE ISNARE HANDLE "BROKE IN HALF" AND THE STENT WAS UNABLE TO DEPLOY. ANOTHER DEVICE WAS UTILIZED FOR THE PATIENT PROCEDURE. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21767025 ↗MalfunctionJul 12, 2023Retraction Problem; Retraction Problem
THE USER FACILITY REPORTED THAT FOLLOWING USE OF THEIR ISNARE SYSTEM - LARIAT SNARES DURING PROCEDURES FOR INJECTIONS THE NEEDLE WOULD NOT RETRACT. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17309890 ↗MalfunctionNov 18, 2022Retraction Problem; Retraction Problem
THE USER FACILITY REPORTED THAT DURING A PROCEDURE WHILE USING THEIR LARIAT SNARE THE NEEDLE WOULD NOT RETRACT. NO INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15828077 ↗
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- Ultratome XL M00535900Boston Scientific Corporation · SNARE, FLEXIBLE205 reports
- CAPTIVATOR M00562340Boston Scientific Corporation · SNARE, FLEXIBLE2 recalls71 reports
- CAPTIVATOR II M00561230Boston Scientific Corporation · SNARE, FLEXIBLE1 recall83 reports
- CAPTIVATOR M00562320Boston Scientific Corporation · SNARE, FLEXIBLE2 recalls32 reports
- CAPTIVATOR M00562300Boston Scientific Corporation · SNARE, FLEXIBLE1 recall78 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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