Admiral AP1-310054Recalls & reported problems
Seaspine Orthopedics Corporation · Cervical Plate, 3 Level, 54mm · Class 2 · Implant
Data updated Oct 13, 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 10889981278311), received between Mar 19, 2026 and Mar 19, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Separation Problem” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Separation Problem1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 19, 2026Separation Problem
A PATIENT UNDERWENT A 3 LEVEL ACDF SPINAL SURGERY ON (B)(6) 2024 CONSISTING OF THE SEASPINE/ORTHOFIX ADMIRAL ACP SYSTEM. SEASPINE/ORTHOFIX WAS MADE AWARE ON 20 FEB 2026 THAT SCREWS BACKED OUT APPROXIMATELY 12 MONTHS POST-OPERATIVELY. THE X-RAY PROVIDED APPEARS TO SHOW THAT ONE OF THE TOP SCREWS (SUPERIOR MOST) HAS BACKED OUT. ADDITIONALLY, ONE OF THE INFERIOR-MOST SCREWS (CAUDAL SCREWS) APPEARS TO BE SLIGHTLY MORE PROMINENT COMPARED TO THE OTHERS. THE PART NUMBERS THAT WERE REPORTED WERE AP1-714018 4.0MM VARIABLE ANGLE SCREW AND A AP1-310054 CERVICAL PLATE, 3 LEVEL, 54MM. NO PATIENT INJURY WAS REPORTED. CURRENTLY, THE PATIENT IS BEING MONITORED BY THE SURGEON, AND NO REVISION SURGERY IS PLANNED. THIS REPORT IS BEING FILED FOR THE AP1-310054 CERVICAL PLATE, 3 LEVEL, 54MM. SEE 3012120772-2026-00012 REPORT FOR THE AP1-714018 4.0MM VARIABLE ANGLE SCREW, SELF-DRILLING, 18MM.
Patient problems: Insufficient Information
MAUDE report 24644374 ↗
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
- Elegance® Anterior Cervical Plate 53430353Clariance · Appliance, Fixation, Spinal Intervertebral Body1 recall0 reports
- Elegance® Anterior Cervical Plate 53430108Clariance · Appliance, Fixation, Spinal Intervertebral Body1 recall0 reports
- Elegance® Anterior Cervical Plate 53430114Clariance · Appliance, Fixation, Spinal Intervertebral Body1 recall0 reports
- Elegance® Anterior Cervical Plate 53430240Clariance · Appliance, Fixation, Spinal Intervertebral Body1 recall0 reports
- Elegance® Anterior Cervical Plate 53430236Clariance · 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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