Centurion DT21830BRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10653160353461), received between Nov 18, 2025 and May 5, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (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.

• MalfunctionMay 5, 2026Break

  IT WAS REPORTED THAT ON 3/23/2026, "RN REPORTED BROKEN STERILE NS SYRINGE, FROM IVAD ACCESS KIT."

  Patient problems: Unspecified Tissue Injury

  MAUDE report 25086846 ↗
• MalfunctionNov 18, 2025Break; Material Integrity Problem; Break; Material Integrity Problem

  ACCORDING TO THE FACILITY, WHEN THE NURSE WAS ACCESSING A PATIENT'S PORT, "RN WENT TO TRY AND FLUSH THE PORT. UPON FLUSHING THE PORT AFTER VERIFYING BLOOD RETURN THE FINGER HOLD ON TO THE FLUSH CRACKED OFF. THIS RESULTED IN THE PLASTIC ON THE SYRINGE CUTTING THROUGH THE STERILE GLOVES AND CAUSING A CUT TO THE RN RIGHT INDEX FINGER." PER THE FACILITY, PATIENT'S PORT WAS EXPOSED LONGER THAN NEEDED, HOWEVER "NOTHING HAPPENED." FOR THE USER, "NO FOLLOW UP CARE NEEDED. WASHED WOUND WITH SOAP AND WATER AND COVERED WITH BAND AIDE. MONITORED FOR S/S OF INFECTION. WOUND IS HEALED." FACILITY ALSO REPORTS "PLUNGER RETRACTS ALL THE WAY OUT OF THE BARREL."

  Patient problems: Laceration(s)

  MAUDE report 23582070 ↗