CARDINAL HEALTH PC24CGSVCRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10887488810898), received between May 10, 2018 and May 10, 2018 — classified as 1 injury.

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

• InjuryMay 10, 2018Material Fragmentation

  THE CUSTOMER STATED THAT THE JACKSON PRATT DRAIN TUBING (B)(4) FROM THE CABG KIT/ (B)(4) BROKE WHEN BEING REMOVED WAS RETAINED INSIDE THE CHEST OF THE PATIENT. THE PATIENT WAS TAKEN BACK TO CARDIOVASCULAR OPERATING ROOM TO HAVE THE DRAIN SURGICALLY REMOVED UNDER GENERAL ANESTHESIA WHERE ALL PIECES WERE RETRIEVED.

  Patient problems: Device Embedded In Tissue or Plaque

  MAUDE report 7504533 ↗