Centurion ECVC1525Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10653160253457), received between Sep 28, 2026 and Sep 30, 2026 — classified as 5 malfunctions.

The most frequently reported specific device problem is “Infusion or Flow Problem” (5 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 30, 2026Infusion or Flow Problem

  It was reported that "Blood return not present on blue and white lumen, minimally present on brown port with positioning and laying patient supine."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50947492 ↗
• MalfunctionSep 30, 2026Infusion or Flow Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50947447 ↗
• MalfunctionSep 30, 2026Infusion or Flow Problem

  It was reported that "L IJ TLC. Only brown port with blood return. All ports able to be flushed."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50947344 ↗
• MalfunctionSep 30, 2026Use of Device Problem; Infusion or Flow Problem

  It was reported that "New triple lumen catheter does not have blood return" and "By 5/4, no blood return present in any of the ports".

  Patient problems: Needle Stick/Puncture

  MAUDE report 50947285 ↗
• MalfunctionSep 28, 2026Infusion or Flow Problem

  It was reported that "no blood return from white port" and "unable to get blood return from white port again."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50913334 ↗