EMERGE Anterior Cervical Plate System 100-4L74Recalls & reported problems
Evolution Spine LLC · 4 LEVEL PLATE 74 mm · Class 2 · Implant
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 00195860013151), received between Jan 8, 2024 and Jan 8, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Misassembly by Users” (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.
Reports received per month
Most reported problems
Device problems
- Misassembly by Users1
Patient problems
- Failure of Implant1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 8, 2024Misassembly by Users; Misassembly by Users
THE PRIMARY SURGERY OCCURRED ON (B)(6) 023. EVOLUTION WAS CONDUCTING A CADAVER LAB WITH THE DOCTOR (ON AN UNRELATED PROJECT) ON (B)(6) 2023 (DATE OF AWARENESS) AND HE MENTIONED THAT HE HAD A COVER COME OFF OF AN EMERGE PLATE. THE DOCTOR DID NOT PROVIDE ANY IMAGES OR ADDITIONAL DETAILS OTHER THAN THAT THE LOWEST PLATE COVER WAS SHOWN AS DISPLACED ON A ROUTINE FOLLOW-UP X-RAY. THE DOCTOR SAID THAT THE PATIENT IS STILL BEING MONITORED. NO REVISION HAS BEEN SCHEDULED.
Patient problems: Failure of Implant
MAUDE report 18470292 ↗
Other Appliance, fixation, spinal intervertebral body devices
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- 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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