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Map-iT 901670Recalls & reported problems

Access Point Technologies, Inc. · Steerable Duo-Decapolar Catheter, Multi-Purpose D Curve-DL · Class 2

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 00818087020220), received between Aug 18, 2020 and Aug 18, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Difficult to Remove” (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

  • Difficult to Remove1

Patient problems

  • No Code Available1

Recent adverse event reports

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

  • MalfunctionAug 18, 2020Difficult to Remove; Difficult to Remove

    IN THE MIDDLE OF CASE, THE CURVE LOCKED AND COULD NOT BE STRAIGHTENED OUT EVEN THOUGH THE USER MOVED IT IN MANY WAYS. THE HANDLE WAS CUT OFF AND A LONG SHEATH WAS PLACED TO REMOVE THE CATHETER. THERE WERE NO PATIENT CONSEQUENCES REPORTED.

    Patient problems: No Code Available

    MAUDE report 10420161 ↗

Other Catheter, Electrode Recording, Or Probe, Electrode Recording devices

All Catheter, Electrode Recording, Or Probe, Electrode Recording devices →

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