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Beacon Tip Torcon NB G09751Recalls & reported problems

Cook Incorporated · Beacon Tip Torcon NB Advantage Catheter · Class 2

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
1

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00827002097513), received between Jul 22, 2022 and Jul 22, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (1 report).

1 FDA recall record name this device's identifier, 1 still open.

1 other recall cover devices cleared under the same FDA submission (K173289); they may or may not involve this specific model.

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.

Recalls naming this device

  1. May 15, 2025Open, Classified

    Cook Medical identified that catheters supplied in the affected device lots may experience tip separation.

    Z-1902-2025 · Root cause: Process change control · FDA record ↗

Most reported problems

Device problems

  • Break1

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.

  • InjuryJul 22, 2022Break; Break

    AS REPORTED, UPON SUCCESSFUL COMPLETION OF A FISTULA DE-CLOTTING PROCEDURE IN THE UPPER ARM, THE TIP OF A BEACON TIP TORCON NB ADVANTAGE ANGIOGRAPHIC CATHETER SEPARATED AND REMAINS IN THE PATIENT. PER THE USER, THE VESSEL IS TOO SMALL TO RETRIEVE THE DEVICE, WHICH REPORTEDLY WILL BE UNABLE TO MIGRATE DUE TO THE SMALL SIZE OF THE VESSEL. THE PATIENT DID NOT REQUIRE ANY ADDITIONAL PROCEDURES DUE TO THIS OCCURRENCE. ACCORDING TO THE INITIAL REPORTER, THE PATIENT DID NOT EXPERIENCE ANY ADVERSE EFFECTS DUE TO THIS OCCURRENCE.

    Patient problems: Foreign Body In Patient

    MAUDE report 15085921 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K173289. One submission often covers many models, so check the product and lot details in each record.

  • Z-1936-2026 · Apr 2, 2026 · Open, Classified
    Beacon Tip Centimeter Sizing Catheter RPN/GPN NR5.0-35-70-P-10S-0-CSC-20 G31213 NR5.0-35-100-P-10S-0-CSC-20 G31214 NR5.0-35-100-P-10S-PIG-CSC-20 G31216 NR5.0-35-70-P-10S-VCF-CSC-20

Other CATHETER, INTRAVASCULAR, DIAGNOSTIC devices

All CATHETER, INTRAVASCULAR, DIAGNOSTIC devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.