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CARDINAL HEALTH SNE21BSDCHRecalls & reported problems

Cardinal Health 200, LLC · RMC NEURO · Class 1

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

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10888439398649), received between Apr 26, 2021 and Apr 26, 2021 — classified as 1 malfunction.

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

Device problems

  • Material Frayed1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionApr 26, 2021Material Frayed; Material Frayed

    CUSTOMER REPORTED THE SPONGE GAUZE(C-NXR4416A) FROM NEUROLOGICAL TRAY(SNE21BSDCH) WAS UNRAVELING DURING LUMBAR DISC PROCEDURE. THE GAUZE SPONGE WAS USED FOR REMOVAL AND BLOTTING OF BLOOD AND FLUIDS DURING THE PROCEDURE. REPORTEDLY, FRAYING FROM THE GAUZE SPONGE WAS FOUND ON THE PATIENT AND ON SCRUB TECH¿S HANDS. THERE WAS NO INJURY, ADVERSE EFFECT OR COMPLICATIONS. NO PATIENT DEMOGRAPHICS WERE PROVIDED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11729536 ↗

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Sources and updates

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