CARDINAL HEALTH BCA200Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10885380182945), received between May 8, 2024 and Apr 14, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (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 16, 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.

• MalfunctionApr 14, 2026Component Incompatible

  WHEN USING TO DRAW LABS FROM IV, THE ADAPTER IS CAUSING BLOOD COLLECTION TUBES TO POP OFF. THE TUBES FEEL PRESSURIZED AND BLOOD SPRAYS ON THE PATIENT. THIS IS FOR MULTIPLE DIFFERENT BLOOD TUBES MAINLY WITHOUT GEL/MEDIUM. MULTIPLE TUBES WERE USED BEFORE THE FAILURE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24870247 ↗
• MalfunctionMay 8, 2024Break; Break

  PLEASE FIND A NEW COMPLAINT ATTACHED FROM A CARDINAL CUSTOMER REGARDING A BROKEN LUER HUB. BASED ON THE DESCRIPTION AND LOT INFORMATION PROVIDED IT APPEARS TO BE ANOTHER ALCOHOL-RELATED ISSUE, BUT WE WILL REQUEST ADDITIONAL INFORMATION ON HOW IT WAS USED AND WHAT IT WAS USED WITH AND SHARE ALL FEEDBACK WITH YOU ONCE WE RECEIVE A RESPONSE FROM THE CUSTOMER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19266037 ↗