Centurion 67365Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00653160115123), received between Sep 21, 2026 and Sep 29, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Dull, Blunt” (3 reports).

1 FDA recall record name this device's identifier, 1 still open.

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.

Recalls naming this device

1. Feb 23, 2024Open, Classified

   Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.

   Z-1441-2024 · Root cause: Process control · FDA record ↗

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 29, 2026Dull, Blunt

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50932162 ↗
• MalfunctionSep 25, 2026Dull, Blunt

  It was reported that "Many of these are coming in dull."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50899285 ↗
• MalfunctionSep 21, 2026Dull, Blunt

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50841407 ↗