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Aero-LL 48941310Recalls & reported problems

Stryker Corporation · Lumbar Cage System · Class 2 · Implant

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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 07613327068153), received between Sep 7, 2016 and Sep 7, 2016 — classified as 1 injury.

The most frequently reported specific device problem is “Bent” (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 18, 2026.

Most reported problems

Device problems

  • Bent1
  • Material Deformation1

Patient problems

  • No Information1
  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjurySep 7, 2016Bent; Material Deformation; Material Deformation

    IT WAS REPORTED THAT THE IMPLANT WAS USED ON A PATIENT WITH ADJACENT SEGMENT DISEASE. THE ANCHOR WAS APPROX. 30% INTO THE VERTEBRAL BODY WHEN IT BEGAN TO BEND.

    Patient problems: No Information; No Known Impact Or Consequence To Patient

    MAUDE report 5934048 ↗

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Sources and updates

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