Mobi-C Plug & Fit US MB3574Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 03662663059084), received between Sep 18, 2024 and Oct 15, 2025 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (4 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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionOct 15, 2025Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THAT A MOBI-C IMPLANT WAS NOT PERFORMING AS INTENDED AND APPEARED TO BE COMING APART IN-SITU. A NEW IMPLANT WAS USED THAT WITH NO ISSUE AND THERE WAS NO PATIENT HARM OR PROCEDURAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23303311 ↗
• MalfunctionJan 22, 2025Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THAT DURING A SURGERY, THE SURGEON ENCOUNTERED EXCESSIVE PLAY WITH THE ATTACHMENT BETWEEN THE IMPLANT AND INSERTER FOR TWO IMPLANTS, RESULTING IN BOTH BEING DISLODGED FROM PEEK, WITH THE INFERIOR PORTION OF THE IMPLANTS REMAINING INTACT TO PEEK. THE SURGERY WAS COMPLETED WITH A THIRD IMPLANT, AND WITHOUT HARM OR DELAYS. THIS IS REPORT TWO OF TWO FOR THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21209529 ↗
• MalfunctionJan 22, 2025Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THAT DURING A SURGERY, THE SURGEON ENCOUNTERED EXCESSIVE PLAY WITH THE ATTACHMENT BETWEEN THE IMPLANT AND INSERTER FOR TWO IMPLANTS, RESULTING IN BOTH BEING DISLODGED FROM PEEK, WITH THE INFERIOR PORTION OF THE IMPLANTS REMAINING INTACT TO PEEK. THE SURGERY WAS COMPLETED WITH A THIRD IMPLANT, AND WITHOUT HARM OR DELAYS. THIS IS REPORT ONE OF TWO FOR THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21209518 ↗
• MalfunctionSep 18, 2024Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THAT A MOBI-C IMPLANT DISASSEMBLED DURING IMPLANTATION. THE IMPLANT WAS DISCARDED AND A NEW IMPLANT WAS USED; THERE WAS NO PATIENT IMPACT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20248894 ↗