Mobi-C® Plug & Fit US MB3376Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 03662663000109), received between Sep 8, 2021 and Jul 1, 2024 — classified as 3 injuries.

The most frequently reported specific device problem is “Migration” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryJul 1, 2024Fracture; Migration; Fracture; Migration

  A PATIENT REPORTED THAT A MOBI-C IMPLANTED AT C6/7 APPROXIMATELY 9 YEARS PRIOR HAD BROKEN DURING THEIR SLEEP; THE MOBILE CORE FRACTURED. THE PATIENT ALLEGED INTENSE PAIN FOR SEVERAL WEEKS PRIOR TO EMERGENCY SURGERY TO CORRECT PARALYSIS AND A LIFE THREATENING CONDITION. THE MOBI-C WAS REMOVED AND THE PATIENT WAS CONVERTED TO A FUSION.

  Patient problems: Pain; Paralysis; Paresthesia

  MAUDE report 19652398 ↗
• InjuryAug 5, 2022Migration or Expulsion of Device; Migration or Expulsion of Device

  IT WAS REPORTED THAT A MOBI-C IMPLANT MIGRATED ANTERIORLY POST-OPERATIVELY. A REVISION SURGERY WAS PERFORMED WHERE THE DEVICE WAS REMOVED AND REPLACED WITH ANOTHER MOBI-C OF THE SAME SIZE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15178764 ↗
• InjurySep 8, 2021Migration; Migration

  IT WAS REPORTED THAT A REVISION SURGERY WAS PERFORMED TO ADDRESS DEVICE MIGRATION FOUND DURING A 6-WEEK POST-OPERATION FOLLOW-UP. BOTH MOBI-C DEVICES WERE REMOVED AND REPLACED BY A FUSION CONSTRUCT DURING THE REVISION. THIS IS REPORT ONE OF TWO FOR THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12439578 ↗