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SUPER TORQUE 532598ARecalls & reported problems

Cordis Corporation · CATH MB 5F PIG 110CM 6SH · Class 2

Data updated Oct 13, 2026 from official FDA records · Editorial policy

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10705032012027), received between Mar 3, 2020 and Mar 3, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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

  • Detachment of Device or Device Component1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMar 3, 2020Detachment of Device or Device Component; Detachment of Device or Device Component

    AS REPORTED, ONE OF THE GOLDEN ROUND MARKER BANDS OF AN ANGIOGRAPHIC 5F X 110CM SUPERTORQUE CATHETER WAS MISSING. THERE WAS NO REPORTED PATIENT INJURY. THEY DON`T KNOW THAT THE DEVICE¿S MARKER BAND WAS MISSING BEFORE THEY USED IT, OR IF IT DISAPPEARED UNDER THE PROCEDURE. THE PATIENT WAS FINE, AND EVERYTHING WAS OK. THE DEVICE IS EXPECTED TO BE RETURNED FOR EVALUATION.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 9780231 ↗

Other CATHETER, INTRAVASCULAR, DIAGNOSTIC devices

All CATHETER, INTRAVASCULAR, DIAGNOSTIC devices →

Sources and updates

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