Lasso 1180-03Recalls & reported problems
Diversatek Healthcare, Inc. · Lasso Polypectomy Snare · Class 2
Data updated Oct 13, 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 00816734021583), received between Jan 6, 2023 and Jan 6, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Use of Device Problem” (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
- Use of Device Problem1
Patient problems
- Perforation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 6, 2023Use of Device Problem; Use of Device Problem
CUSTOMER REPORTED THIS ADVERSE EVENT TO IMPORTER ON DECEMBER 8, 2022. CUSTOMER REPORTED A PERFORATION DURING THE REMOVAL OF POLYPS FROM THE COLON. THE PROCEDURE BEING PERFORMED WAS A COLONSCOPY WITH A POLYPECTOMY X 2 (SIGMOID AND RECTAL). THE ADVERSE EVENT REQUIRED A REPORTED SURGICAL INTERVENTION TO REPAIR THE PERFORATION. THE PATIENT HAD NO REPORTED UNDERLYING HEALTH ISSUES THAT MAY HAVE CONTRIBUTED TO THE EVENT. THE PATIENT WAS HOSPITALIZED FOR 4 DAYS TOTAL.
Patient problems: Perforation
MAUDE report 16112415 ↗
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- CAPTIVATOR II M00561230Boston Scientific Corporation · SNARE, FLEXIBLE1 recall83 reports
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- 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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