Conquest® CQ7552Recalls & reported problems
Bard Peripheral Vascular, Inc. · Conquest® PTA Balloon Dilatation Catheter 5 mm x 20 mm, 75 cm catheter · Class 2
All models of Conquest (32)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741062827), received between Apr 16, 2020 and May 9, 2025 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Break” (2 reports).
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.
Reports received per month
Most reported problems
Device problems
- Break2
- Deflation Problem1
- Difficult to Remove1
- Material Deformation1
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- 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.
InjuryMay 9, 2025Break; Deflation Problem; Difficult to Remove; Break; Deflation Problem; Difficult to Remove
ON (B)(6) 2025, A PATIENT UNDERWENT A PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) PROCEDURE USING THE CONQUEST PTA BALLOON CATHETER. DURING THE PROCEDURE, THE BALLOON CATHETER ALLEGEDLY CANNOT BE REMOVED AFTER USE. IT WAS FURTHER REPORTED THE BALLOON WAS BREAK IN AN ATTEMPT TO REMOVE IT, BUT IT WAS STILL UNSUCCESSFUL. REPORTEDLY, THE BALLOON WAS ULTIMATELY REMOVED SURGICALLY, AND THE BALLOON WAS NOT COMPLETELY DEFLATED. THERE WERE NO COMPLICATIONS.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 21991863 ↗MalfunctionApr 16, 2020Break; Material Deformation; Break; Material Deformation
THIS REPORT SUMMARIZES ONE MALFUNCTION. THE INFORMATION REVIEWED INDICATED THAT MODEL CQ7552 PTA BALLOON DILATATION CATHETER ALLEGEDLY EXPERIENCED MATERIAL DEFORMATION AND BREAK. THE INFORMATION WAS RECEIVED FROM ONE SOURCE THE MALFUNCTION DID NOT INVOLVE A PATIENT. PATIENT INFORMATION WAS NOT PROVIDED.
Patient problems: No Patient Involvement
MAUDE report 9967638 ↗
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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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