Conquest® CQ75122Recalls & reported problems
Bard Peripheral Vascular, Inc. · Conquest® PTA Balloon Dilatation Catheter 12 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
- 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 00801741063244), received between Apr 25, 2022 and Apr 25, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Deflation Problem” (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
- Deflation Problem1
- Entrapment of Device1
- Inflation Problem1
- Material Deformation1
- Material Twisted/Bent1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 25, 2022Deflation Problem; Entrapment of Device; Inflation Problem; Material Deformation; Material Twisted/Bent; Deflation Problem; Entrapment of Device; Inflation Problem; Material Deformation; Material Twisted/Bent
IT WAS REPORTED THAT DURING AN ANGIOPLASTY PROCEDURE, THE PTA BALLOON ALLEGEDLY FAILED TO INFLATE AND DEFLATE. IT WAS FURTHER REPORTED THAT THE BALLOON ALLEGEDLY GOT STRUCK IN THE PATIENT. IT WAS FURTHER REPORTED THAT THE BALLOON DEFLATED BY PUNCTURING OUTSIDE WITH THE HELP OF ULTRASOUND. REPORTEDLY, THE SURGERY TIME INCREASED BY TWO HOURS LONGER AND IT WAS NOT NECESSARY TO OPEN THE PATIENT TO REMOVE THE MATERIAL. THERE WAS NO REPORTED PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14191588 ↗
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- WATCHMAN™ TruSeal™ Access System M635TU70020Boston Scientific Corporation · Catheter, percutaneous1 recall11 deaths217 reports
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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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