CREO 7067.7055Recalls & reported problems
Globus Medical, Inc. · 4.75mm Curved Rod, Cobalt Chrome, 55mm Length · Class 2
All models of CREO (100)
Data updated Oct 16, 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 00889095196221), received between Feb 5, 2026 and Feb 5, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fracture” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Fracture1
Patient problems
- Nonunion/Delayed-union Bone Fracture1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 5, 2026Fracture
THE PATIENT HAD AN L4-S1 INTERBODY FUSION WITH THE CREO 4.75 SCREW SYSTEM ON (B)(6) 2023. THE PATIENT RETURNED TO THE SURGEON IN LATE 2025 FOR PAIN. SURGEON DETERMINED THE PATIENT HAD ADJACENT LEVEL DISEASE AT L3-4 AND POSSIBLY AN IMMATURE FUSION FROM THE PREVIOUS SURGERY AT L4-S1. THE PATIENT WAS SCHEDULED FOR AN L3-4 POSTERIOR INTERBODY FUSION, WHICH WAS DONE ON (B)(6) 2026. DURING THE SURGERY ON (B)(6) IT WAS DETERMINED THAT ONE OF THE PREVIOUSLY PLACED 4.75 COBALT CHROME RODS WAS BROKEN, AND THE PATIENT HAD NOT FULLY HEALED/FUSED FROM THE ORIGINAL SURGERY.
Patient problems: Nonunion/Delayed-union Bone Fracture
MAUDE report 24270694 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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