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CARDINAL HEALTH SNE73NITA6Recalls & reported problems

Cardinal Health 200, LLC · NEURO INTERVENTIONAL PACK · Class 1

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10888439877175), received between Nov 25, 2020 and Nov 25, 2020 — classified as 2 malfunctions.

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

Device problems

  • Appropriate Device Problem Term/Code Not Available2

Patient problems

  • No Clinical Signs, Symptoms or Conditions2

Recent adverse event reports

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

  • MalfunctionNov 25, 2020Appropriate Device Problem Term/Code Not Available

    CUSTOMER REPORTED EXCESSIVE LINTING OF BLUE COTTON TOWEL IN THE PACK FOUND DURING CEREBRAL ANGIOGRAM WITH INTERVENTION. THERE WAS NO INJURY OR ADVERSE EFFECT DUE TO EXCESSIVE LINT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 10899856 ↗
  • MalfunctionNov 25, 2020Appropriate Device Problem Term/Code Not Available

    CUSTOMER REPORTED EXCESSIVE LINTING OF BLUE COTTON TOWEL IN THE PACK FOUND DURING CEREBRAL ANGIOGRAM WITH INTERVENTION. THERE WAS NO INJURY OR ADVERSE EFFECT DUE TO EXCESSIVE LINT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 10899755 ↗

Other Neurological tray devices

All Neurological tray devices →

Sources and updates

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