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AVS Anchor-L 48663128Recalls & reported problems

Stryker Corporation · VERTEBRAL SPACER · Class 2 · Implant

Data updated Oct 18, 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 07613252602194), received between Oct 10, 2016 and Oct 10, 2016 — classified as 1 malfunction.

The most frequently reported specific device problem is “Malposition of Device” (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

  • Adverse Event Without Identified Device or Use Problem1
  • Malposition of Device1

Patient problems

  • 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.

  • MalfunctionOct 10, 2016Adverse Event Without Identified Device or Use Problem; Malposition of Device; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT; SCREW WENT THROUGH THE CAGE. YES, REPLACEMENT HARDWARE WAS USED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 6015099 ↗

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Sources and updates

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