Brevia Short Term Dialysis Catheter 5565150Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741045462), received between Dec 9, 2015 and Dec 9, 2015 — classified as 1 malfunction.

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. What reports can and can't tell you · How this data works · Data updated Oct 18, 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.

• MalfunctionDec 9, 2015Device Dislodged or Dislocated

  FACILITY REPORTED TO SALES REPRESENTATIVE THAT WHEN PHYSICIAN WENT TO PLACE CATHETER, THE SPRING ALLEGEDLY DISLODGED PRIOR TO USE. SALES REPRESENTATIVE TRIED CONTACTING THE PHYSICIAN FOR ADDITIONAL DETAILS BUT HAS NOT YET HEARD BACK. THE FACILITY REPORTED THAT THE SPRING HAD SOMETHING TO WITH THE NEEDLE IN THE KIT. PHYSICIAN WAS SAID TO HAVE OPENED ANOTHER KIT TO COMPLETE THE PROCEDURE. NO PATIENT INVOLVEMENT REPORTED AS THIS WAS SAID TO HAVE HAPPENED BEFORE PLACEMENT. ON (B)(6) 2015 - RETURNED SAMPLE SHOWS BLOOD RESIDUE INDICATING THIS DEVICE WAS USED ON A PATIENT.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 5282766 ↗