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
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 ↗
Other Laparoscope, general & plastic surgery devices
- HIGH DEFINITION LCD MONITOR OEV262HOlympus Medical Systems Corp. · Laparoscope, general & plastic surgery1,937 reports
- HD AUTOCLAVABLE CAMERA HEAD OTV-S7ProH-HD-12EOlympus Medical Systems Corp. · Laparoscope, general & plastic surgery1,886 reports
- HD AUTOCLAVABLE CAMERA HEAD OTV-S7ProH-HD-10EOlympus Medical Systems Corp. · Laparoscope, general & plastic surgery1,086 reports
- Auto Suture OMS-T10BTCovidien LP · Laparoscope, general & plastic surgery1 recall955 reports
- PDB OMS-PDB1000Covidien LP · Laparoscope, general & plastic surgery859 reports
- VISERA 4K UHD CAMERA CONTROL UNIT OLYMPUS OTV-S400Olympus Medical Systems Corp. · Laparoscope, general & plastic surgery777 reports
- Auto Suture OMS-T10SBCovidien LP · Laparoscope, general & plastic surgery1 recall697 reports
- Spacemaker SMBTTRNDXCovidien LP · Laparoscope, general & plastic surgery590 reports
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page