Port Access Needle S02120-75Recalls & reported problems
Bard Access Systems, Inc. · MiniLoc 20G x 0.75 inch with y-site · Class 2
All models of Port Access Needle (122)
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 00801741087721), received between Jan 27, 2021 and Jan 27, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Disconnection” (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
- Disconnection1
- Leak/Splash1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 27, 2021Disconnection; Leak/Splash
IT WAS REPORTED THAT AFTER FLUSHING THE DEVICE, THE SMALL CAP LOCATED BETWEEN THE TWO CLAMPS ON THE EXTENSION TUBING ALLEGEDLY CAME OFF AND THE PATIENT GOT BLOOD AND SALINE ON THEIR SHIRT AND CONSEQUENTLY, THE SYSTEM WAS OPEN TO AIR. ADDITIONAL INFORMATION RECEIVED 8 JAN 2021: IT WAS REPORTED THE CLAMPS WERE BOTH CLAMPED AND A CAP WAS PUT ON THE END TO CLOSE IT OFF. NO PATIENT HARM WAS REPORTED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 11241006 ↗
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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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