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DeRoyal 89-5560Recalls & reported problems

Deroyal Industries, Inc. · CATARACT TRAY · Class 2

Data updated Oct 13, 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 00749756644792), received between Jun 8, 2018 and Jun 8, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Contamination With Biological Material” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Device Contamination With Biological Material1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • MalfunctionJun 8, 2018Device Contamination With Biological Material

    WHEN OPENING THE EYE PACK FOR A CASE, A SMALL INSECT WAS NOTICED ON TOP OF THE INSIDE OF THE PACK. THE PACK, AS WELL AS SUPPLIES OPENED, WERE THROWN AWAY. ROOM CLEANED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7581993 ↗

Other General surgery tray devices

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Sources and updates

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