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CONVERTORS 8378Recalls & reported problems

Cardinal Health 200, LLC · Table Cover · Class 2

All models of CONVERTORS (38)

Data updated Oct 16, 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 10885380118678), received between Jul 28, 2020 and Jul 28, 2020 — classified as 1 malfunction.

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 16, 2026.

Most reported problems

Device problems

  • Contamination /Decontamination Problem1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionJul 28, 2020Contamination /Decontamination Problem

    THE OPERATING ROOM TECH FOUND A DEAD BUG WHEN OPENING A CARDINAL HEALTH 200 CONVERTORS TABLE COVER FOR A TOTAL KNEE ARTHROPLASTY. THE CONTAMINATED TABLE COVER WAS IMMEDIATELY DISCHARGED FROM THE OR AND A NEW DEVICE WAS OPENED TO CONTINUE THE ORIGINAL INTENDED PROCEDURE. NOTHING ELSE WAS CONTAMINATED DURING THE INCIDENT.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 10331830 ↗

Other Drape, surgical, exempt devices

All Drape, surgical, exempt devices →

Sources and updates

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