CARDINAL HEALTH SAN12CCMWSRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10887488822198), received between Feb 5, 2019 and Feb 5, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Contamination /Decontamination Problem” (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.

• MalfunctionFeb 5, 2019Contamination /Decontamination Problem

  THE CUSTOMER REPORTED THAT LINT FROM THE BLUE OR TOWELS PWTB03-STMA FROM THE HEART CATHETER TRAY KIT/ SAN12CCMWS WAS FOUND ON THE PHYSICIAN¿S HANDS AND IN THE IRRIGATION BOWL DURING A LEFT CARDIAC CATHETERIZATION. THE TOWELS WERE USED TO CLEAN EQUIPMENT. THERE WAS NO INJURY REPORTED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8305017 ↗