McKesson 25-2748Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10612479182353), received between Mar 17, 2026 and Mar 17, 2026 — classified as 2 malfunctions.

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

• MalfunctionMar 17, 2026Separation Problem

  THE CUSTOMER REPORTED THE HEMOSTAT BREAKING WHILE IN USE. THERE WERE NO PATIENT INJURY AND NO MEDICAL INTERVENTION REQUIRED. THE CUSTOMER CONFIRMED THE INSTRUMENT WAS CLAMPEDON THE CATHETER WHEN IT BROKE WHILE REMOVING THE CATHETER DURING ROUTINE PROCEDURE (NOT EMERGENCY PROCEDURE). THERE WAS DELAY OF APPROXIMATELY A FEW MINUTES FOR EACH PROCEDUREINVOLVED DURING CATHETER REMOVAL.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24617399 ↗
• MalfunctionMar 17, 2026Separation Problem

  THE CUSTOMER REPORTED THE HEMOSTAT BREAKING WHILE IN USE. THERE WERE NO PATIENT INJURY AND NO MEDICAL INTERVENTION REQUIRED. THE CUSTOMER CONFIRMED THE INSTRUMENT WAS CLAMPED ON THE CATHETER WHEN IT BROKE WHILE REMOVING THE CATHETER DURING ROUTINE PROCEDURE (NOT EMERGENCY PROCEDURE). THERE WAS DELAY OF APPROXIMATELY A FEW MINUTES FOR EACH PROCEDURE INVOLVED DURING CATHETER REMOVAL.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24617375 ↗