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Quantum™ Maverick™ H7493808020350Recalls & reported problems

Boston Scientific Corporation · PTCA Dilatation Catheter · Class 2

All models of Quantum Maverick (36)

Data updated Oct 18, 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 08714729392910), received between Feb 6, 2020 and Apr 1, 2020 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (2 reports).

5 other recalls cover devices cleared under the same FDA submission (P860019); 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Break2

Patient problems

  • No Consequences Or Impact To Patient1
  • No Patient Involvement1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionApr 1, 2020Break; Break

    IT WAS REPORTED THAT A SHAFT BREAK OCCURRED. DURING A PROCEDURE INVOLVING A 3.5MM X 20MM QUANTUM MAVERICK BALLOON CATHETER, A SHAFT BREAK OCCURRED INSIDE THE PATIENT. THE DEVICE WAS REMOVED WITHOUT ADDITIONAL INTERVENTION AND THERE WAS NO PATIENT INJURY.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 9913536 ↗
  • MalfunctionFeb 6, 2020Break; Break

    IT WAS REPORTED THAT SHAFT BREAK OCCURRED. A 3.5MM X 20MM QUANTUM MAVERICK BALLOON CATHETER WAS SELECTED FOR USE. HOWEVER, AFTER UNPACKING THE DEVICE, IT WAS NOTICED THAT THE SHAFT WAS FRACTURED. NO PATIENT COMPLICATIONS WERE REPORTED AND THE PATIENT WAS STABLE.

    Patient problems: No Patient Involvement

    MAUDE report 9678358 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under P860019. One submission often covers many models, so check the product and lot details in each record.

  • Z-2165-2008 · May 1, 2007 · Terminated
    Boston Scientific Scimed Maverick 2 Monorail" PTCA Catheter, 3.0 mm 15 mm REF 38928-1530 Lot 9565194 Use before 2010-04 Indicated for balloon dilation of the stenotic portion o
  • Z-2166-2008 · Nov 1, 2005 · Terminated
    Boston Scientific Scimed Maverick 2 Monorail 12mm Balloon Catheter, 2.5 mm x 12 mm Made in Ireland Ballybrit Business Park, Galway, Ireland REF 38928-1225 Use before 2007-01 UPN H
  • Z-0032-04 · Aug 20, 2003 · Terminated
    Ace Percutaneous Transluminal Coronary Angioplasty (PTCA) Dilatation Catheter with 1 cm Tip and 20 mm Balloon, Catalog Number H74903628151
  • Z-0031-04 · Aug 20, 2003 · Terminated
    Ace Percutaneous Transluminal Coronary Angioplasty (PTCA) Dilatation Catheter with 2cm Tip 20 mm Balloon, Catalog Number H74902071051
  • Z-0030-04 · Aug 20, 2003 · Terminated
    Ace Percutaneous Transluminal Coronary Angioplasty (PTCA) Dilatation Catheter with 2cm Tip 20 mm Balloon, Catalog Number H74902071011

Other Catheters, transluminal coronary angioplasty, percutaneous devices

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Sources and updates

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