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ANCHORAGE XFR006100Recalls & reported problems

Stryker GmbH · Cross-Plate Reamer · Class 1

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 07613252265771), received between Feb 14, 2019 and Feb 14, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Therapeutic or Diagnostic Output Failure” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Therapeutic or Diagnostic Output Failure1

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.

  • MalfunctionFeb 14, 2019Therapeutic or Diagnostic Output Failure

    WHEN OVER-DRILLING WITH THE RECESSED CUTTERS, ABRASION WAS DETECTED IN THE ANCHORAGE SYSTEM. THERE WERE NO SPECIAL MEASURES TO COMPLETE THE MEDICAL PROCEDURE SUCCESSFULLY. THE ABRASION WAS ONLY REMOVED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 8341360 ↗

Other INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT devices

All INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.