Port Access Needle 0661910Recalls & reported problems
Bard Access Systems, Inc. · LiftLoc 19G x 1 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
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741047800), received between Feb 26, 2019 and Feb 26, 2019 — classified as 1 injury.
The most frequently reported specific device problem is “Fail-Safe Did Not Operate” (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
- Fail-Safe Did Not Operate1
Patient problems
- Needle Stick/Puncture1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryFeb 26, 2019Fail-Safe Did Not Operate
IT WAS REPORTED (B)(4) NEEDLE SAFETY CLOSURE DEVICE FAILED TO CLOSE, LEADING TO A NEEDLE STICK ON AN EMPLOYEE. FACILITY FOLLOWED THE BLOOD BORNE PATHOGEN EXPOSURE PROCEDURE PER FACILITY POLICY AND ALSO INITIATED TREATMENT FOR THE EMPLOYEE AND SENT THE EMPLOYEE TO OUTSIDE FACILITY FOR PROPHYLACTIC TREATMENT. EMPLOYEE WILL CONTINUE TO FOLLOW UP WITH LAB WORK AND PROPHYLACTIC TREATMENT. NO OTHER INFORMATION WAS PROVIDED.
Patient problems: Needle Stick/Puncture
MAUDE report 8371567 ↗
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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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