Torcon NB G31422Recalls & reported problems
Cook Incorporated · Torcon NB, Advantage Catheter · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00827002314221), received between Nov 6, 2018 and Nov 6, 2018 — classified as 1 injury.
The most frequently reported specific device problem is “Material Separation” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Material Separation1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 6, 2018Material Separation; Material Separation
IT WAS REPORTED A TORCON NB ADVANTAGE ANGIOGRAPHIC CATHETER WAS PLACED IN THE PATIENT FOR BILIARY DRAINAGE. DURING THE PROCEDURE, THE TIP OF THE CATHETER SEPARATED IN THE BILIARY DUCT. THE PHYSICIAN USED ANOTHER COMPANY'S GUIDE WIRE TO PUSH THE TIP INTO THE DUODENUM TO BE EXPELLED THROUGH NATURAL MEANS. AS REPORTED, THE PATIENT DID NOT REQUIRE ADDITIONAL PROCEDURES DUE TO THIS OCCURRENCE.
Patient problems: Foreign Body In Patient
MAUDE report 8043639 ↗
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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 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.
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