Centurion I505BF9Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10653160248347), received between Sep 28, 2026 and Sep 29, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 29, 2026Structural Problem; Device Dislodged or Dislocated

  It was reported that "at end of case, it was noted that the suture eyelet had broken and catheter had migrated from original suture site."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50932657 ↗
• MalfunctionSep 28, 2026Migration

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50924709 ↗