Port Access AS142075Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741118272), received between Jul 16, 2021 and Jul 16, 2021 — classified as 2 injuries.

The most frequently reported specific device problem is “Fluid/Blood Leak” (2 reports).

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

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryJul 16, 2021Fluid/Blood Leak; Fluid/Blood Leak

  IT WAS REPORTED "WE HAVE A 3 YEAR OLD THAT NOW HAS HAD 2 TUBING FRACTURES WITH THE POWER NEEDLE IN THE ALL POINTS KITS AND UNFORTUNATELY HE HAS A CONFIRMED CLABSI. RL¿S HAVE BEEN PLACED AND ONE OF THE NEEDLES WAS SENT TO VALUE ANALYSIS." THIS REPORT ADDRESSES THE DEVICE THAT WAS SAVED AND SENT TO VALUE ANALYSIS.

  Patient problems: Unspecified Infection

  MAUDE report 12181022 ↗
• InjuryJul 16, 2021Fluid/Blood Leak; Fluid/Blood Leak

  IT WAS REPORTED "WE HAVE A (B)(6) YEAR OLD THAT NOW HAS HAD 2 TUBING FRACTURES WITH THE POWER NEEDLE IN THE ALL POINTS KITS AND UNFORTUNATELY HE HAS A CONFIRMED CLABSI. RL¿S HAVE BEEN PLACED AND ONE OF THE NEEDLES WAS SENT TO VALUE ANALYSIS." THIS REPORT ADDRESSES THE DEVICE THAT WAS NOT SENT TO VALUE ANALYSIS.

  Patient problems: Unspecified Infection

  MAUDE report 12181021 ↗