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QUARTEX 1149.9200Recalls & reported problems

Globus Medical, Inc. · QUARTEX Occipital Plate, Small · Class 2

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 00889095357936), received between Nov 16, 2020 and Nov 16, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Migration or Expulsion of Device” (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

  • Migration or Expulsion of Device1

Patient problems

  • Failure of Implant1

Recent adverse event reports

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

  • MalfunctionNov 16, 2020Migration or Expulsion of Device

    IT WAS REPORTED THAT A REVISION SURGERY WAS DONE TO REMOVE A QUARTEX OCCIPITAL PLATE, WHICH HAD BACKED OUT POST-OPERATIVELY.

    Patient problems: Failure of Implant

    MAUDE report 10847890 ↗

Other APPLIANCE, FIXATION, SPINAL INTERLAMINAL devices

All APPLIANCE, FIXATION, SPINAL INTERLAMINAL devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.