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Mobi-C® Plug & Fit US MB3557Recalls & reported problems

LDR Spine Usa, Inc. · Total Cervical Disc Replacement System: Mobi-C Cervical Disc Prosthesis · Class 3 · Implant

All models of Mobi-C Plug & Fit US (13)

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

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03662663000086), received between Jun 26, 2019 and Jun 26, 2019 — 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 18, 2026.

Most reported problems

Device problems

  • Detachment of Device or Device Component1
  • Disconnection1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionJun 26, 2019Disconnection; Detachment of Device or Device Component; Disconnection; Detachment of Device or Device Component

    IT WAS REPORTED THAT THE MOBI-C IMPLANT DISASSEMBLED DURING SURGERY, WHILE IMPACTING THE DEVICE INTO THE FINAL LOCATION. THE SURGEON CHOSE TO SWITCH TO FUSION AND NO FURTHER PATIENT IMPACT WAS REPORTED.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8735444 ↗

Other Prosthesis, Intervertebral Disc devices

All Prosthesis, Intervertebral Disc devices →

Sources and updates

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