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Modulus 67940036P2Recalls & reported problems

Nuvasive, Inc. · Modulus Cervical, 6x17x14mm 7° · 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 00887517959416), received between Aug 18, 2020 and Aug 18, 2020 — classified as 1 malfunction.

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.

Most reported problems

Device problems

  • Migration1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionAug 18, 2020Migration; Migration

    A PATIENT UNDERWENT A SPINAL PROCEDURE ON C5-7 LEVELS ON (B)(6) 2019. A POST-OP RADIOGRAPH TAKEN ON AN UNKNOWN DATE REVEALED THAT THE CAGE HAS MIGRATED. THERE ARE NO PLANS FOR A REVISION PROCEDURE PER THE SURGEON.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 10423751 ↗

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