Conquest® 40 CQF7544Recalls & reported problems
Bard Peripheral Vascular, Inc. · Conquest® 40 PTA Dilatation Catheter 4 mm x 40 mm, 75 cm catheter · Class 2
All models of Conquest 40 (25)
Data updated Oct 16, 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 00801741060342), received between Aug 13, 2018 and Aug 13, 2018 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Rupture” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Material Rupture1
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.
MalfunctionAug 13, 2018Material Rupture; Material Rupture
IT WAS REPORTED DURING AN ANGIOPLASTY PROCEDURE OF A LEFT UPPER ARM FISTULA, THE PTA BALLOON ALLEGEDLY RUPTURED AT 15 ATM. THE BALLOON WAS REMOVED IN ITS ENTIRETY THROUGH THE SHEATH WITHOUT DIFFICULTY. THERE WAS NO REPORTED DETACHMENT OF BALLOON MATERIAL NOR ANY VESSEL DAMAGE. THE PROCEDURE WAS COMPLETED WITH ANOTHER BALLOON. THERE WAS NO REPORTED PATIENT INJURY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7779427 ↗
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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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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