Roth Net 00711050 (UDI 00724995182496)Recalls & reported problems
US Endoscopy · The disposable Roth Net foreign body standard retrieval device is used in the endoscopic retrieval of foreign body, food bolus and excised tissue such as polyps. · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 00724995182496), received between Sep 4, 2020 and Feb 13, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component1
- Difficult to Open or Close1
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.
MalfunctionFeb 13, 2026Difficult to Open or Close
THE USER FACILITY REPORTED VIA VIGILANCE REPORT # (B)(4) THAT FOLLOWING THE REMOVAL OF A COIN DURING A GASTROSCOPY, THE NET TO THEIR ROTH NET DEVICE WOULD NOT CLOSE. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24333626 ↗MalfunctionSep 4, 2020Detachment of Device or Device Component
THE DISTRIBUTOR REPORTED THAT THE MESH COMPONENT OF A ROTH NET DEVICE BECAME PARTIALLY DETACHED DURING A PROCEDURE, AND REPORTED THE PROCEDURE WAS NOT COMPLETED. THERE WAS NO REPORT OF HARM TO THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 10495143 ↗
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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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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