FORTIFY 151.153Recalls & reported problems
Globus Medical, Inc. · FORTIFY 20mm Core, Height 41-64mm · 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 00889095043051), received between Jun 17, 2026 and Jun 17, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Collapse” (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.
Reports received per month
Most reported problems
Device problems
- Collapse1
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 17, 2026Collapse
IT WAS REPORTED THAT ON (B)(6) 2026 THE SURGEON ANNOUNCED A NEW FORTIFY COLLAPSE INCIDENT IN CHUV (LUMBAR REGION). THIS INCIDENT WAS DETECTED AFTER A YEARLY POST-OPERATIVE CHECK. THE PATIENT WAS OPERATED ON (B)(6) 2023 AND IS CURRENTLY ASYMPTOMATIC.
Patient problems: Insufficient Information
MAUDE report 25531696 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.