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ACDF Stand Alone Cervical 03.18.118Recalls & reported problems

Medacta International SA · Mecta-C SA TiPEEK Cage 18x15x6x7° · Class 2 · Implant

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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 07630040725729), received between May 12, 2023 and May 12, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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 18, 2026.

Most reported problems

Device problems

  • Detachment of Device or Device Component1

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.

  • InjuryMay 12, 2023Detachment of Device or Device Component; Detachment of Device or Device Component

    DURING THE FOLLOW UP VISIT, THE X-RAYS REVEALED A DISCONNECTION BETWEEN THE CAGE AND THE PLATE. PATIENT IS STABLE AND NON SYMPTOMATIC, THE FUSION OF THE VERTEBRAE APPEARS TO BE CORRECT AND NO REVISION SURGERY HAS BEEN PLANNED. THE SURGEON REPORTED THAT WILL MAINTAIN MONITORED THE PATIENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16917741 ↗

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Sources and updates

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