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RELIEVE 136.704Recalls & reported problems

Globus Medical, Inc. · RELIEVE 2.6mm Screw, Self-Tapping, 4mm · Class 2 · Implant

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 00889095040715), received between Jun 7, 2022 and Jun 7, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Loose or Intermittent Connection” (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

  • Loose or Intermittent Connection1

Patient problems

  • Insufficient Information1

Recent adverse event reports

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

  • MalfunctionJun 7, 2022Loose or Intermittent Connection

    IT WAS REPORTED THAT A RELIEVE SCREW WAS FOUND LOOSENED AT C3 ONE WEEK POST OPERATIVE. THIS EVENT OCCURRED IN JAPAN.

    Patient problems: Insufficient Information

    MAUDE report 14625729 ↗

Other ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL devices

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