Port Access Needle 0672234Recalls & reported problems
Bard Access Systems, Inc. · PowerLoc 22G x 0.75 inch with y-site · Class 2
All models of Port Access Needle (122)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741047978), received between Nov 25, 2019 and Jul 10, 2020 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Crack” (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
- Crack1
- Fluid/Blood Leak1
Patient problems
- No Consequences Or Impact To Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 10, 2020Crack; Crack
IT WAS REPORTED THAT WHEN FLUSHING THE NEEDLE AFTER DRUG WAS INFUSED THE NURSE SAW THE LEAK ON THE PLASTIC HUB.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10257161 ↗MalfunctionNov 25, 2019Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT A SMALL HOLE WAS FOUND IN THE PIGTAIL ABOVE THE CLAMP. NO OTHER INFORMATION WAS PROVIDED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9370380 ↗
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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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