Mobi-C® Plug & Fit US MB3596Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03662663000192), received between Oct 13, 2020 and Oct 13, 2020 — classified as 1 malfunction.

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 16, 2026.

Most reported problems

Recent adverse event reports

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

• MalfunctionOct 13, 2020Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THE SURGEON USED THE MALLET TO TAMP THE IMPLANT INTO PLACE. WHILE THE IMPLANT WAS STILL CONNECTED TO THE INSERTER, THE SURGEON REVIEWED AN X-RAY AND DECIDED HE WANTED TO HAVE THE IMPLANT SIT FURTHER BACK. UPON STRIKING THE INSERTER WITH THE MALLET, THE IMPLANT DISASSEMBLED IN THE DISC SPACE. ALL PIECES WERE RETRIEVED. A NEW IMPLANT WAS SUCCESSFULLY USED TO COMPLETE THE CASE. THERE WERE NO REPORTED IMPACTS ON THE PATIENT.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 10673555 ↗