Lasso 1180-12Recalls & reported problems
Diversatek Healthcare, Inc. · Lasso Polypectomy Snare · Class 1
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00816734023020), received between Feb 13, 2023 and Oct 29, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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
- Detachment of Device or Device Component2
- Break1
- Fracture1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 29, 2025Break; Detachment of Device or Device Component; Break; Detachment of Device or Device Component
NO ADVERSE EVENT RELATED TO THIS INCIDENT. IT WAS REPORTED TO DIVERSATEK HEALTHCARE THAT A COLD ONLY SNARE COMPLETELY BROKE OFF INSIDE OF A PATIENT WHILE TRYING TO CUT A POLYP. THE WHOLE LOOP FELL OFF WHEN THE SNARE WAS CLOSED. THE WIRE PIECE WAS RETRIEVED AND NO PATIENT INJURY WAS NOTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23416816 ↗MalfunctionFeb 13, 2023Fracture; Detachment of Device or Device Component; Fracture; Detachment of Device or Device Component
NO ADVERSE EVENT RELATED TO THIS INCIDENT. AS THE SNARE WAS CLOSING AROUND THE POLYP, THE SNARE WIRE BROKE OFF FROM THE CATHETER. THE WIRE PIECE WAS RETRIEVED WITH A BIOPSY FORCEPS AND NO PATIENT INJURY WAS NOTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16364994 ↗
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- Single Use Electrosurgical Snare SD-400 SD-400U-15Olympus Medical Systems Corp. · SNARE, NON-ELECTRICAL1 recall7 reports
- M-Catch 1175-01Diversatek Healthcare, Inc. · Snare, Non-Electrical1 recall0 reports
- Exacto 00711115US Endoscopy · SNARE, NON-ELECTRICAL35 reports
- CAPTIVATOR II M00561240Boston Scientific Corporation · SNARE, NON-ELECTRICAL26 reports
- Single Use Electrosurgical Snare SD-400 SD-400-10Olympus Medical Systems Corp. · SNARE, NON-ELECTRICAL16 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.