Admiral AP1-200030Recalls & reported problems
Seaspine Orthopedics Corporation · Cervical Plate, 2 Level, 30mm · Class 2 · Implant
All models of Admiral (19)
Data updated Oct 16, 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 10889981238216), received between Feb 7, 2023 and Feb 7, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Premature Separation” (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 16, 2026.
Most reported problems
Device problems
- Premature Separation1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 7, 2023Premature Separation; Premature Separation
A PATIENT UNDERWENT SPINAL SURGERY CONSISTING OF SEASPINE'S ADMIRAL PLATE SYSTEMS. THE INDEX SURGERY DATE WAS ON (B)(6) 2022. SEASPINE WAS MADE AWARE ON (B)(6) 2023 THAT A SCREW BACK OUT HAD OCCURRED. THE REPORTER NOTED THAT DURING THE INDEX SURGERY AN AP1-200030 CERVICAL PLATE, 2 LEVEL, 30MM WAS NOT ABLE TO CAM LOCK OVER THE SCREW TO FINAL LOCK. THEY ONLY HAD AN ISSUE ON ONE OF THE DISTAL ENDS OF THE PLATE. DURING A PHONE CALL ON (B)(6) 2023 WITH SEASPINE, THE REPORTER STATED THAT THE SURGEON DECIDED TO LEAVE THE PLATE IN PLACE AND COMPLETED THE INDEX SURGERY. HOWEVER, 4 MONTHS POSTOP THE SCREW BACKED OUT. THEN A REVISION SURGERY WAS PERFORMED ON (B)(6) 2023 TO CORRECT THE ISSUE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16313577 ↗
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
- 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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