Roth Net Platinum 00715160Recalls & reported problems
US Endoscopy · The disposable Roth Net Platinum polyp, sterile retrieval device product line 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
- 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 00724995182939), received between Jul 11, 2025 and Jul 11, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Difficult to Remove” (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
- Difficult to Remove1
- Mechanical Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 11, 2025Mechanical Problem; Difficult to Remove; Mechanical Problem; Difficult to Remove
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE, THE NET FROM THEIR ROTH NET PLATINUM GOT CAUGHT ON A CLIP THAT HAD BEEN PLACED AT THE BASE OF THE POLYP IN THE COLON. USER FACILITY PERSONNEL CUT THE NET AT THE HANDLE OUTSIDE OF THE PATIENT TO REMOVE THE COLONOSCOPE FROM THE PATIENT. THE POLYPS WERE SUCCESSFULLY REMOVED AND RETRIEVED. IT WAS CONFIRMED DURING A FOLLOW-UP APPOINTMENT THAT THE NET WAS NOT PRESENT IN THE PATIENT. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22478781 ↗
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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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