CREO 7067.7040Recalls & reported problems
Globus Medical, Inc. · 4.75mm Curved Rod, Cobalt Chrome, 40mm Length · Class 2
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00889095196191), received between Jan 16, 2025 and Apr 2, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fracture” (2 reports).
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
- Fracture2
Patient problems
- Insufficient Information1
- Spinal Column Injury1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 2, 2025Fracture; Fracture
IT WAS REPORTED THAT A REVISION WAS NEEDED TO REPLACE A BROKEN CREO 4.75MM CURVED ROD THAT WAS CAUSING PATIENT PAIN POST OPERATIVELY.
Patient problems: Spinal Column Injury
MAUDE report 21752405 ↗MalfunctionJan 16, 2025Fracture; Fracture
IT WAS REPORTED THAT A REVISION WAS NEEDED TO REPLACE A CREO ROD WAS FOUND BROKEN POST OPERATIVELY.
Patient problems: Insufficient Information
MAUDE report 21171906 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.