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AVS Anchor-C 48335308Recalls & reported problems

Stryker Corporation · SELF-DRILLING SCREW · Class 2 · Implant

All models of AVS Anchor-C (10)

Data updated Oct 16, 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 04546540679826), received between Apr 13, 2016 and Apr 13, 2016 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (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 16, 2026.

Most reported problems

Device problems

  • Break2
  • Detachment Of Device Component1
  • Mechanical Problem1

Patient problems

  • No Known Impact Or Consequence To Patient2

Recent adverse event reports

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

  • MalfunctionApr 13, 2016Break

    IT WAS REPORTED THAT THE COLLARS BROKEN ON BOTH SCREWS. REPLACED WITH NEW ONES.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 5574786 ↗
  • MalfunctionApr 13, 2016Break; Detachment Of Device Component; Mechanical Problem; Detachment Of Device Component; Mechanical Problem

    IT WAS REPORTED THAT THE COLLARS BROKEN ON BOTH SCREWS. REPLACED WITH NEW ONES.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 5574785 ↗

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Sources and updates

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