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Admiral AP1-210028Recalls & reported problems

Seaspine Orthopedics Corporation · Cervical Plate, 2 Level, 28mm · Class 2 · Implant

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10889981278113), received between Aug 8, 2023 and Aug 8, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Unstable” (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.

Most reported problems

Device problems

  • Unstable1

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.

  • InjuryAug 8, 2023Unstable; Unstable

    ON (B)(6)2023, IT WAS REPORTED THAT A SURGEON EXPERIENCED DIFFICULTY DURING AN ACDF C5-C7 PERFORMED ON (B)(6)2023 WITH THE LOCKING MECHANISM ON AN AP1-210028 CERVICAL PLATE, 2 LEVEL, 28MM. NO EXPLANTS WILL BE RETURNED. THE SURGEON BENT THE PLATE BUT NOT OVER THE LOCKING MECHANISM. THE SURGEON WAS ABLE TO LOCK C5 AND C7 BUT C6 SPUN FREELY WITH NO RESISTANCE WHEN TURNING THE COVER. IT WAS OBSERVED THAT THE COVER WAS NOT SITTING PROUD.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17484737 ↗

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.