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AVS Anchor-C 48325310Recalls & reported problems

Stryker Corporation · SELF-TAPPING 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
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 04546540679758), received between Mar 9, 2016 and Mar 9, 2016 — classified as 1 malfunction.

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

Most reported problems

Device problems

  • Break1
  • Failure to Advance1

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.

  • MalfunctionMar 9, 2016Break; Failure to Advance

    IT WAS REPORTED THAT WHILE PLACING A SCREW INTO THE CAGE, THE SCREW STOPPED ADVANCING AND THE LOCKING RING ON THE SCREW BROKE. THE APPROPRIATE GUIDE WAS BEING USED. THE HOLE FOR THE SCREW HAD BEEN PREPARED WITH BOTH AN AWL AND DRILL.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 5490028 ↗

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Sources and updates

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