Admiral AP1-310051Recalls & reported problems
Seaspine Orthopedics Corporation · Cervical Plate, 3 Level, 51mm · Class 2 · Implant
All models of Admiral (19)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10889981278304), received between Mar 7, 2025 and Mar 3, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Separation Problem” (2 reports).
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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Separation Problem2
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 3, 2026Separation Problem
A PATIENT UNDERWENT A 3 LEVEL ACDF SPINAL SURGERY ON (B)(6) 2025 CONSISTING OF THE SEASPINE/ORTHOFIX ADMIRAL ACP SYSTEM. SEASPINE/ORTHOFIX WAS MADE AWARE ON 06 FEB 2026 THAT ONE OF THE INFERIOR-MOST SCREWS (CAUDAL SCREWS) BACKED OUT, APPROXIMATELY 6 MONTHS POST-OPERATIVELY. THE PART NUMBERS THAT WERE REPORTED WERE A AP1-714018 4.0MM VARIABLE ANGLE SCREW AND A AP1-310051 CERVICAL PLATE, 3 LEVEL, 51MM. THE REPORTER NOTED THAT THE LOCKING COVERS OF THE AP1-310051 CERVICAL PLATE APPEARED TO HAVE BEEN APPROPRIATELY ENGAGED AT THE COMPLETION OF THE INDEX SURGERY. 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 AP1-310051 CERVICAL PLATE. SEE 3012120772-2026-00007 REPORT FOR THE AP1-714018 4.0MM VARIABLE ANGLE SCREW, SELF-DRILLING, 18MM.
Patient problems: Insufficient Information
MAUDE report 24499640 ↗MalfunctionMar 7, 2025Separation Problem; Separation Problem
ON (B)(6) 2024, A PATIENT UNDERWENT CERVICAL SPINAL SURGERY CONSISTING OF THE ADMIRAL ACP SYSTEM. ON (B)(6) 2025, IT WAS REPORTED THAT THE ADMIRAL CERVICAL PLATE FAILED TO SECURE A MATING SCREW, LEADING TO A SCREW BACKOUT DURING THE POSTOPERATIVE PERIOD.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21548111 ↗
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
- Mariner RDX MX1-000040Seaspine Orthopedics Corporation · Appliance, fixation, spinal intervertebral body1 recall0 reports
- Mariner RDX MX1-000030Seaspine Orthopedics Corporation · Appliance, fixation, spinal intervertebral body1 recall0 reports
- Elegance® Anterior Cervical Plate 53430112Clariance · Appliance, Fixation, Spinal Intervertebral Body1 recall0 reports
- Elegance® Anterior Cervical Plate 53430224Clariance · Appliance, Fixation, Spinal Intervertebral Body1 recall0 reports
- XLP 7565050Nuvasive, Inc. · 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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