BD Prevue II Peripheral Vascular Access System 9770700RRecalls & reported problems
Bard Access Systems, Inc. · BD Prevue II Console (Refurbished) · 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
- 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 00801741214929), received between Nov 15, 2023 and Nov 15, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Defective Component” (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
- Defective Component1
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.
MalfunctionNov 15, 2023Defective Component; Defective Component
IT WAS FOUND DURING EVALUATION AT BD SERVICE FACILITY THAT THERE ARE DARK HORIZONTAL LINES IN THE ULTRASOUND IMAGE DUE TO AN INTERNAL FAILURE WITHIN THE RFID ANTENNA CAUSING INTERFERENCE WITH THE BEAMFORMER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18139393 ↗
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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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