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DeRoyal 89-8813Recalls & reported problems

Deroyal Industries, Inc. · KEESLER ARTHROGRAM TRAY - RXPGY · Class 2

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 00749756890045), received between Dec 6, 2018 and Dec 6, 2018 — classified as 1 malfunction.

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

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Pain1

Recent adverse event reports

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

  • MalfunctionDec 6, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    "A" ARTHROGRAM KIT CONTAINED LIDOCAINE THAT DID NOT SEEM EFFECTIVE. A PATIENT REPORTEDLY EXPERIENCED PAIN AS A RESULT, AND THE DOCTOR INJECTED ADDITIONAL MEDICATION THAT DID NOT SEEM TO WORK. THIS RESULTED IN THE PHYSICIAN PULLING AN ADDITIONAL BOTTLE OF LIDOCAINE, WHICH WAS EFFECTIVE.

    Patient problems: Pain

    MAUDE report 8138083 ↗

Other General surgery tray devices

All General surgery tray devices →

Sources and updates

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