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AVS Anchor-L 48992001Recalls & reported problems

Stryker Corporation · IMPLANT HOLDER · Class 2

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 07613252602774), received between Aug 17, 2017 and Aug 17, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Difficult to Remove” (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

  • Difficult to Remove1

Patient problems

  • No Consequences Or Impact To Patient1
  • 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.

  • MalfunctionAug 17, 2017Difficult to Remove

    IT WAS REPORTED THAT; DURING SURGERY AFTER RELEASING THE LEVER IMPLANT INSERTER COULD NOT BE REMOVED FROM IMPLANT. IMPLANT WAS ABLE TO REMOVE FROM THE INSERTER BY PULLING SIDE OUT WITH NERVE HOOK.

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

    MAUDE report 6800029 ↗

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Sources and updates

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