Roth Net 00711057 (UDI 00816765010891)Recalls & reported problems
US Endoscopy · The disposable Roth Net foreign body mini retrieval device is used in the endoscopic retrieval of foreign body, food bolus and excised tissue such as polyps. · Class 2
Data updated Oct 13, 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 00816765010891), received between Oct 3, 2018 and Nov 9, 2018 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (2 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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Detachment of Device or Device Component2
- Break1
Patient problems
- No Known Impact Or Consequence To Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 9, 2018Detachment of Device or Device Component
US ENDOSCOPY RECEIVED MEDWATCH # (B)(4) REPORTING THAT DURING AN ESOPHAGOGASTRODUODENOSCOPY (EGD) FOR FOREIGN BODY REMOVAL, THE PHYSICIAN WAS ATTEMPTING TO REMOVE THE FOREIGN BODY SPECIMEN WHEN THE NETTING BROKE AWAY FROM THE LOOPING. THE EVENT WAS RECTIFIED, HOWEVER ON SECOND ATTEMPT THE SAME OCCURRED AGAIN. THERE WAS NO REPORT OF PATIENT OR USER HARM.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8054549 ↗MalfunctionOct 3, 2018Break; Detachment of Device or Device Component
DURING ESOPHAGOGASTRODUODENOSCOPY (EGD) FOR FOREIGN BODY REMOVAL, THE PHYSICIAN WAS ATTEMPTING TO REMOVE THE FOREIGN BODY SPECIMEN WHEN THE NETTING BROKE AWAY FROM THE LOOPING. EVENT WAS RECTIFIED, HOWEVER ON SECOND ATTEMPT THE SAME OCCURRED AGAIN.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7929365 ↗
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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 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