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Aero-LL 48942208Recalls & reported problems

Stryker Corporation · Lumbar Cage System · Class 2 · Implant

Data updated Oct 18, 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 07613327065848), received between Jun 27, 2016 and Jun 13, 2017 — classified as 2 malfunctions.

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

Most reported problems

Device problems

  • Bent2
  • Material Deformation1

Patient problems

  • No Known Impact Or Consequence To Patient2
  • No Information1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJun 13, 2017Bent; Material Deformation; Material Deformation

    IT WAS REPORTED THAT; SURGEON HAD COMPLETED INSERTION OF CAGE INTO LUMBAR DISC SPACE. WANTED TO PUT ONE ANCHOR IN SUPERIORLY, ANCHOR IMPLANT BENT AGAINST HARD OSTEOPHYTE AND SURGEON WAS FORCED TO PUT ANCHOR IN INFERIORLY.

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

    MAUDE report 6638279 ↗
  • MalfunctionJun 27, 2016Bent

    IT WAS REPORTED THAT THE PILOT CUTTER AND THE CAGE BLADE BENT, USED A REPLACEMENT DEVICE

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 5753072 ↗

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Sources and updates

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