CARDINAL HEALTH SCV73OHDSDRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10888439631432), received between Jul 1, 2020 and Jul 1, 2020 — classified as 2 malfunctions.

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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 1, 2020Contamination /Decontamination Problem

  CUSTOMER REPORTED THAT DURING AN OPEN HEART PROCEDURE, LINT FROM THE OR TOWELS PWTB04-STM FROM THE HEART PACK SCV73OHDSD WAS FOUND ON THE INSTRUMENTS, GLOVES, AND ON THE ARMS OF TEAMMATES THAT USED THE TOWELS TO DRY GLOVED HANDS. THERE WAS NO DELAY IN PROCEDURE AND NO INJURY. NO PATIENT DEMOGRAPHICS WERE PROVIDED UPON REQUEST.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 10218587 ↗
• MalfunctionJul 1, 2020Material Fragmentation

  CUSTOMER REPORTED THAT DURING AN OPEN HEART PROCEDURE THE LAP SPONGES LS1818PSA FROM THE HEART PACK SCV73OHDSD HAD A LOT OF LINT SO THEY WERE REMOVED AND NOT USED FOR THE CASE. THERE WAS NO DELAY AND NO INJURY. NO PATIENT DEMOGRAPHICS WERE PROVIDED UPON REQUEST.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10218318 ↗