Lariat 00711119 (UDI 00816765012550)Recalls & reported problems
US Endoscopy · The Lariat snare is an electrosurgical device used to endoscopically grasp, dissect, and transect tissue during Gastrointestinal (GI) endoscopic procedures. The snare can be used with or without the use of monopolar diathermic energy. · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00816765012550), received between Jul 25, 2019 and Jul 25, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Entrapment of Device” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Entrapment of Device1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 25, 2019Entrapment of Device
THE USER FACILITY REPORTED THAT, DURING PIECEMEAL RESECTION OF A 7-8 CM POLYP IN THE COLON, THE SNARE LOOP OF A LARIAT SNARE BECAME ENTRAPPED IN THE POLYP TISSUE. THE USER ATTEMPTED TO DISENGAGE THE SNARE FROM THE POLYP WITHOUT SUCCESS AND AN ADDITIONAL PROCEDURE WAS REQUIRED TO REMOVE THE SNARE AND COMPLETE THE POLYPECTOMY. THE PATIENT IS REPORTED TO BE WELL.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8825832 ↗
Other SNARE, FLEXIBLE devices
- CAPTIFLEX M00562400Boston Scientific Corporation · SNARE, FLEXIBLE3 recalls85 reports
- SENSATION Short Throw M00562670Boston Scientific Corporation · SNARE, FLEXIBLE1 recall178 reports
- SENSATION Short Throw M00562650Boston Scientific Corporation · SNARE, FLEXIBLE1 recall173 reports
- 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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