Centurion ECVC6690Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10653160320432), received between Sep 29, 2026 and Sep 29, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Split, Cut or Torn” (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

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 29, 2026Material Split, Cut or Torn

  It was reported that "the probe cover inside the medline central line kit is splitting down the seam when being secured, thus causing a break in sterile field."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50934831 ↗