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MC+ MC322PRecalls & reported problems

LDR Spine Usa, Inc. · CLOSED CERVICAL CAGE 14X15.5 H6 mm · Class 2

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 03662663021432), received between May 22, 2023 and May 22, 2023 — classified as 2 injuries.

The most frequently reported specific device problem is “Biocompatibility” (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.

Most reported problems

Device problems

  • Biocompatibility2

Patient problems

  • Inflammation2
  • Pain2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryMay 22, 2023Biocompatibility; Biocompatibility

    A PATIENT REPORTED INFLAMMATION AND CHRONIC PAIN DUE TO THE METALS OR PLASTIC COMPONENTS IN TWO MC+ CAGES AND PLATES. THE CONSTRUCTS REMAIN IMPLANTED. THIS IS REPORT FOUR OF FOUR FOR THIS EVENT.

    Patient problems: Inflammation; Pain

    MAUDE report 16973591 ↗
  • InjuryMay 22, 2023Biocompatibility; Biocompatibility

    A PATIENT REPORTED INFLAMMATION AND CHRONIC PAIN DUE TO THE METALS OR PLASTIC COMPONENTS IN TWO MC+ CAGES AND PLATES. THE CONSTRUCTS REMAIN IMPLANTED. THIS IS REPORT THREE OF FOUR FOR THIS EVENT.

    Patient problems: Inflammation; Pain

    MAUDE report 16973584 ↗

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