Admiral AP1-704014Recalls & reported problems
Seaspine Orthopedics Corporation · 4.0mm Variable Angle Screw, Self-Tapping, 14mm · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10889981278823), received between Jun 2, 2025 and Jun 2, 2025 — classified as 2 injuries.
The most frequently reported specific device problem is “Fracture” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Fracture2
Patient problems
- Insufficient Information2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJun 2, 2025Fracture; Fracture
ON 05 MAY 2025, SEASPINE/ORTHOFIX WAS MADE AWARE OF A REVISION SURGERY DUE TO A SCREW THAT BACKED OUT OF AN ADMIRAL CERVICAL PLATE CONSTRUCT. THE PROVIDED X-RAY CORROBORATES THE REPORT. TWO SCREWS AND THE PLATE'S INFERIOR LOCKING COVER WERE REMOVED. THE SURGEON CHOSE TO LEAVE THE PLATE AND REMAINING SCREWS IN-SITU. NO PATIENT INJURY WAS REPORTED. THIS REPORT IS FOR 1 OF 2 AP1-704014 4.0MM VARIABLE ANGLE SCREWS, SELF-TAPPING, 14MM. THE AP1-310045 CERVICAL PLATE, 3 LEVEL, 45MM WAS REPORTED ON 3012120772-2025-00034.
Patient problems: Insufficient Information
MAUDE report 22127702 ↗InjuryJun 2, 2025Fracture; Fracture
ON (B)(6) 2025, SEASPINE/ORTHOFIX WAS MADE AWARE OF A REVISION SURGERY DUE TO A SCREW THAT BACKED OUT OF AN ADMIRAL CERVICAL PLATE CONSTRUCT. THE PROVIDED X-RAY CORROBORATES THE REPORT. TWO SCREWS AND THE PLATE'S INFERIOR LOCKING COVER WERE REMOVED. THE SURGEON CHOSE TO LEAVE THE PLATE AND REMAINING SCREWS IN-SITU. NO PATIENT INJURY WAS REPORTED. THIS REPORT IS FOR 2 OF 2 AP1-704014 4.0MM VARIABLE ANGLE SCREWS, SELF-TAPPING, 14MM. THE AP1-310045 CERVICAL PLATE, 3 LEVEL, 45MM WAS REPORTED ON 3012120772-2025-00034.
Patient problems: Insufficient Information
MAUDE report 22127688 ↗
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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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