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Roth Net Platinum 00715050 (UDI 00724995182908)Recalls & reported problems

US Endoscopy · The disposable Roth Net Platinum universal 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 18, 2026 from official FDA records · Editorial policy

Adverse event reports
8
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 00724995182908), received between Oct 2, 2020 and Apr 15, 2026 — classified as 8 malfunctions.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (5 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 1 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 1 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 1 reportsSep 2025: 1 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 2 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520262
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Detachment of Device or Device Component5
  • Difficult to Open or Close1
  • Mechanical Problem1
  • Use of Device Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions8

Recent adverse event reports

The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.

  • MalfunctionApr 15, 2026Detachment of Device or Device Component

    THE USER FACILITY REPORTED THAT DURING USE OF THE NET TO THEIR ROTH NET PLATINUM BROKE OFF. THE NET WAS REMOVED WITH ANOTHER DEVICE, AND THEN PROCEDURE WAS COMPLETED SUCCESSFULLY. NO REPORT OF INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24888627 ↗
  • MalfunctionApr 9, 2026Detachment of Device or Device Component

    THE USER FACILITY REPORTED VIA VIGILANCE REPORT (B)(4), THAT DURING USE OF THE NET TO THEIR ROTH NET PLATINUM BROKE OFF. THE NET WAS RETRIEVED, AND THE PROCEDURE WAS COMPLETED SUCCESSFULLY USING A DIFFERENT ROTH NET. NO REPORT OF INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24831368 ↗
  • MalfunctionSep 5, 2025Detachment of Device or Device Component; Detachment of Device or Device Component

    THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THEIR ROTH NET PLATINUM DETACHED FROM THE DEVICE. THE PROCEDURE WAS COMPLETED SUCCESSFULLY USING A GRASPER. NO REPORT OF INJURY OR PROCEDURE DELAY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 22976343 ↗
  • MalfunctionAug 21, 2025Detachment of Device or Device Component; Detachment of Device or Device Component

    THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE, THE NET TO THEIR ROTH NET PLATINUM DETACHED INSIDE A PATIENT. THE NET WAS RETRIEVED, AND THE PROCEDURE WAS COMPLETED SUCCESSFULLY USING A DIFFERENT ROTH NET. NO REPORT OF INJURY OR DELAY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 22864179 ↗
  • MalfunctionDec 12, 2024Mechanical Problem; Mechanical Problem

    THE USER FACILITY REPORTED THAT DURING POLYP RETRIEVAL, THE NET COMPONENT OF THE ROTH NET BECAME STUCK ON THE RESIDUAL POLYP REQUIRING INTERVENTION TO RELEASE THE NET. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO REPORT OF INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 20915799 ↗
  • MalfunctionAug 21, 2024Use of Device Problem; Use of Device Problem

    THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE, THEIR ROTH NET PLATINUM DEVICE GOT STUCK ON THE PATIENT'S TISSUE. USER FACILITY PERSONNEL UTILIZED ANOTHER ROTH NET PLATINUM DEVICE RESULTING IN A PROCEDURE DELAY. THE PATIENT PROCEDURE WAS COMPLETED SUCCESSFULLY. NO REPORT OF INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 20010080 ↗
  • MalfunctionAug 10, 2023Difficult to Open or Close; Difficult to Open or Close

    THE USER FACILITY REPORTED THAT TWO OF THEIR ROTH NETS WERE HAVING DIFFICULTY OPENING AND/OR CLOSING RESULTING IN A PROCEDURE DELAY. A THIRD ROTH NET WAS USED WHICH FUNCTIONED AS INTENDED AND THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO REPORT OF INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17497502 ↗
  • MalfunctionOct 2, 2020Detachment of Device or Device Component

    THE DISTRIBUTOR REPORTED THAT THE WIRE LOOP COMPONENT OF A ROTH NET PLATINUM RETRIEVER - UNIVERSAL DEVICE DETACHED DURING A PATIENT PROCEDURE IN THE COLON. THE WIRE LOOP WAS RETRIEVED, THE PROCEDURE WAS COMPLETED, AND NO HARM TO THE PATIENT OR USER WAS REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 10621313 ↗

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Sources and updates

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