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ANCHORAGE XTV008001Recalls & reported problems

Stryker GmbH · Screwdriver bit, T8, AO quick coupling · Class 1

All models of ANCHORAGE (52)

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 07613252266952), received between Sep 23, 2020 and Sep 23, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fracture” (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

  • Fracture1

Patient problems

  • Foreign Body In Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 23, 2020Fracture; Fracture

    AS REPORTED: "USING MMI ANCHORAGE MTP CP PLATE, WHILE USING THE DISTAL LOCKING GUIDE A 2.0MM DRILL BIT TIP BROKE OFF IN THE PATIENT AND WE WERE UNABLE TO RECOVER IT. ALONG WITH THE DRILL BIT WHILE SCREWING IN THE LAST 3.5MM LOCKING SCREW THE T8 SCREWDRIVER TIP BROKE OFF IN THE SCREW HEAD UNABLE TO GET LOOSE AND OUT OF THE SCREW HEAD. BOTH DRILL BIT AND SCREWDRIVER HEAD STUCK IN THE SCREW WERE LEFT IN THE PATIENT AND SURGICAL SITE CLOSED." NO DELAY¿S OR MAJOR DISTRACTION TO THE CASE.

    Patient problems: Foreign Body In Patient

    MAUDE report 10573141 ↗

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Sources and updates

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