Roth Net 00711170Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00816765013519), received between Feb 21, 2020 and Jan 7, 2021 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Difficult to Open or Close” (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.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionJan 7, 2021Difficult to Open or Close

  STERIS ENDOSCOPY RECEIVED AN ANONYMOUS MEDWATCH REPORT (MW5097835) WHICH REPORTED THAT A ROTH NET WOULD NOT FULLY CLOSE DURING A PROCEDURE. THE REPORT STATED THAT THERE WAS NO HARM TO THE PATIENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11133819 ↗
• MalfunctionFeb 21, 2020Difficult to Open or Close

  A USER FACILITY REPORTED THROUGH THE DISTRIBUTOR IN (B)(6) THAT, AFTER SEVERAL PASSES IN A FOREIGN BODY RETRIEVAL PROCEDURE, A ROTH NET DEVICE BECAME DIFFICULT TO CLOSE. NO HARM TO THE PATIENT OR USER WAS REPORTED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9739718 ↗