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BRYAN® Cervical Disc System 6470314Recalls & reported problems

Medtronic Sofamor Danek, Inc. · MOTION 6470314 14MM BRYAN CRV DSC PRSTHS · Class 3 · Implant

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

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00613994181206), received between Sep 27, 2019 and Sep 27, 2019 — classified as 1 injury.

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

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Reaction1

Recent adverse event reports

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

  • InjurySep 27, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT POST-OP, PATIENT SUFFERED WITH UNSPECIFIED ALLERGY AFTER IMPLANTED DISC SURGERY. THE SURGEON DOES NOT BELIEVE THAT THE ALLERGIC SYMPTOMS WERE RELATED TO THE DISC, WHICH WAS IMPLANTED IN PATIENT FOR 2 YEARS.

    Patient problems: Reaction

    MAUDE report 9132016 ↗

Other PROSTHESIS, INTERVERTEBRAL DISC devices

All PROSTHESIS, INTERVERTEBRAL DISC devices →

Sources and updates

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