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ASSY, SPINAL TABLE TOP, 500LBS 5840-831Recalls & reported problems

Mizuho Orthopedic Systems, Inc. · 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 00842430114427), received between Oct 20, 2021 and Oct 20, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Loss of or Failure to Bond” (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

  • Loss of or Failure to Bond1

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.

  • MalfunctionOct 20, 2021Loss of or Failure to Bond; Loss of or Failure to Bond

    WITH PATIENT PRONE ON TABLE AND SURGERY IN PROGRESS, THE TABLETOP BROKE APART AND FELL ONTO THE C-ARM. NO INJURIES.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12666025 ↗

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Sources and updates

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