ATLANTIS® Anterior Cervical Plate System 7200042Recalls & reported problems
Medtronic Sofamor Danek, Inc. · PLATE 7200042 ATL VISION ELITE 42.5MM · Class 2 · Implant
All models of ATLANTIS Anterior Cervical Plate System (46)
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 00613994625113), received between May 10, 2018 and May 10, 2018 — 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
- Fatigue1
- Headache1
- Increased Sensitivity1
- Inflammation1
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 10, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT PATIENT UNDERWENT SURGERY ON (B)(6) 2013. POST-OP, PATIENT WAS IN CHRONIC PAIN. PATIENT HAS REPORTEDLY PAIN IN NECK, THORACIC AND BACK WHICH HAS PROGRESSED THROUGHOUT THE BODY. PATIENT IS SENSITIVE TO NICKEL AND THE SENSITIVITY IS ALL TIME HIGH. PATIENT ALSO REPORTED TO HAVE ITCHING AND HAS HIVES DUE TO THIS ALLERGY. PATIENT REPORTED GASTRO ISSUES, MAJOR INFLAMMATION ALL OVER PATIENT'S BODY, EXTREME FATIGUE, SEVERE HEADACHES, SENSATION OF ELECTRICITY THAT FEELS LIKE IT IS BURNING & SHARP PAIN, EXTREME FATIGUE, DO NOT FEEL RIGHT AND MANY OTHER SYMPTOMS.
Patient problems: Fatigue; Headache; Increased Sensitivity; Inflammation; Pain
MAUDE report 7501735 ↗
Other APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY devices
- CD HORIZON® SOLERA® VOYAGER™ Spinal System 6550017Medtronic Sofamor Danek, Inc. · Appliance, fixation, spinal intervertebral body131 reports
- EVEREST® Spinal System 2901-10001VB Spine LLC · APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY119 reports
- ZEVO™ Anterior Cervical Plate System 7710015Medtronic Sofamor Danek, Inc. · APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 recall1 report
- XLP 7565050Nuvasive, Inc. · APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 recall0 reports
- Elegance® Anterior Cervical Plate 53430344Clariance · Appliance, Fixation, Spinal Intervertebral Body1 recall0 reports
- ATLANTIS® Anterior Cervical Plate System 876-170Medtronic Sofamor Danek, Inc. · APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 recall0 reports
- XLP 7565060Nuvasive, Inc. · APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 recall0 reports
- Elegance® Anterior Cervical Plate 53430113Clariance · Appliance, Fixation, Spinal Intervertebral Body1 recall0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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