BD Prevue II Peripheral Vascular Access System 9770704Recalls & reported problems
Bard Access Systems, Inc. · BD Prevue II Vascular Access Probe · Class 2
All models of BD Prevue II Peripheral Vascular Access System (6)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00801741214974), received between Sep 5, 2024 and Apr 6, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Break” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
- No Apparent Adverse Event1
- Poor Quality Image1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 6, 2026Break
IT WAS REPORTED THAT WIRES EXPOSED FROM STRAIN RELIEF. NO FURTHER DETAILS PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24794107 ↗MalfunctionFeb 26, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE IMAGE HAS POOR QUALITY. NO OTHER INFORMATION PROVIDED, AT THIS TIME.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21474627 ↗MalfunctionSep 5, 2024Poor Quality Image; Poor Quality Image
IT WAS REPORTED PROBE PRODUCING SPOT ON IMAGES. SWAPPED PROBE AND ISSUE WENT AWAY. NO OTHER INFORMATION WAS PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20152261 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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