Roth Net Platinum 00711155 (UDI 00816765011270)Recalls & reported problems
US Endoscopy · The disposable Roth Net Platinum food bolus retrieval device is used in the endoscopic retrieval food bolus. · Class 2
Data updated Oct 18, 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 00816765011270), received between Oct 31, 2018 and Mar 20, 2019 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Obstruction of Flow” (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 18, 2026.
Most reported problems
Device problems
- Obstruction of Flow1
- Retraction Problem1
Patient problems
- Abrasion1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 20, 2019Retraction Problem
THE USER FACILITY REPORTED THAT DURING RETRIEVAL OF A FOOD BOLUS IN THE ESOPHAGUS, THE USER COULD NOT RETRACT THE ROTH NET DEVICE, REQUIRING DEVICE WITHDRAWAL WITH THE NET LOOP DEPLOYED. THE PROCEDURE CONTINUED WITH A SECOND ROTH NET DEVICE, WHICH ALSO COULD NOT BE RETRACTED. THE FOOD BOLUS PROCEDURE WAS THEN COMPLETED WITH A THIRD RETRIEVAL DEVICE. ESOPHAGEAL SCRAPING WAS REPORTED; HOWEVER, NO TREATMENT WAS REQUIRED AS A RESULT. THE PROCEDURE WAS COMPLETED SUCCESSFULLY.
Patient problems: Abrasion
MAUDE report 8438204 ↗MalfunctionOct 31, 2018Obstruction of Flow
THE USER FACILITY REPORTED THE ROTH NET DEVICE BECAME OBSTRUCTED BY AN ESOPHAGEAL STRICTURE DURING A FOOD BOLUS REMOVAL PROCEDURE, PREVENTING THE DEVICE WITHDRAWAL AND RESULTING IN A PROCEDURAL DELAY. THE PROCEDURE WAS COMPLETED WITH NO REPORTED HARM TO THE USER OR PATIENT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8025624 ↗
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- CAPTIVATOR II M00561230Boston Scientific Corporation · SNARE, FLEXIBLE1 recall83 reports
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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