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CARDINAL HEALTH SEY6VEYPEDRecalls & reported problems

Cardinal Health 200, LLC · EYE PACK 1030 · Class 2

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

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10888439016475), received between Dec 21, 2018 and Dec 21, 2018 — classified as 1 injury.

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

  • Abrasion1
  • Corneal Abrasion1

Recent adverse event reports

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

  • InjuryDec 21, 2018Material Frayed

    FRAYING OF THE DRAPE CAUSED CORNEAL ABRASIONS AND STICKY ADHESIVE CAUSED SKIN ABRASIONS.

    Patient problems: Abrasion; Corneal Abrasion

    MAUDE report 8191350 ↗

Other Eye tray devices

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Sources and updates

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