Port Access Needle 012012Recalls & reported problems
Bard Access Systems, Inc. · HuberPlus 20G x 1.25" · Class 2
- 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 00801741065583), received between Aug 2, 2019 and Aug 2, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Activation Problem” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Activation Problem1
- Protective Measures Problem1
Patient problems
- No Consequences Or Impact To Patient1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 2, 2019Activation Problem; Protective Measures Problem; Activation Problem
IT WAS REPORTED THAT WHEN REMOVING THE HUBER NEEDLE, THE NEEDLE DID NOT ENTER THE SAFETY SYSTEM. THE NURSE PRICKED HERSELF WITH THE NEEDLE AND THEREFORE UNDERWENT AN AES.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 8854958 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.