Modulus 67940000P2Recalls & reported problems
Nuvasive, Inc. · Modulus Cervical, 5x15x12mm 7° · Class 2 · Implant
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887517984104), received between Feb 18, 2025 and Feb 18, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Migration” (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
- Migration1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryFeb 18, 2025Migration; Migration
ON AN UNKNOWN DATE A PATIENT UNDERWENT AN ANTERIOR CERVICAL DISCECTOMY AND FUSION (ACDF) PROCEDURE ON C3/4. ON AN UNKNOWN DATE IT WAS IDENTIFIED THAT THE IMPLANTED INTERBODY SPACE HAD DISLODGED ANTERIORLY. ON (B)(6) 2024, A REVISION PROCEDURE WAS CONDUCTED TO RE-IMPLANT THE CAGE INTO THE PROPER POSITION AND ADD ADDITIONAL STABILIZATION IN THE FORM OF A PLATE. NO ADDITIONAL PATIENT IMPACT WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21403138 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.