VACCESS LT LONG-TERM HEMODIALYSIS CATHETER PLUS 5143230Recalls & reported problems
Bard Access Systems, Inc. · VACCESS PLUS, ST, 16 FR. 23cm · Class 2 · Implant
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 00801741010972), received between Nov 28, 2016 and Nov 28, 2016 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (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.
Most reported problems
Device problems
- Device Contamination with Chemical or Other Material1
- Device Operates Differently Than Expected1
Patient problems
- No Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 28, 2016Device Operates Differently Than Expected; Device Contamination with Chemical or Other Material
FACILITY REPORTED THAT PATIENT'S CATHETER WAS NOT WORKING WELL, WHEN THE HEALTHCARE PROFESSIONAL REMOVED THE DEVICE THEY FOUND A "PLASTIC PIECE" IN THE TIP OF THE CATHETER.
Patient problems: No Information
MAUDE report 6128735 ↗
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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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