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Xia 3 System - Serrato 48268012Recalls & reported problems

Stryker Corporation · Screwdriver Outer Sleeve · Class 1

All models of Xia 3 System - Serrato (36)

Data updated Oct 18, 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 07613327356649), received between May 2, 2018 and May 2, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Crack” (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 18, 2026.

Most reported problems

Device problems

  • Crack1
  • Difficult 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.

  • MalfunctionMay 2, 2018Difficult to Advance; Crack; Difficult to Advance

    IT WAS REPORTED THAT THE THREADS CRACKED ON THE OUTER SLEEVE OF THE SCREWDRIVER. COULD NOT THREAD SCREWDRIVER INTO TULIP HEAD. THERE ARE NO REPORTS OF ADVERSE CONSEQUENCES TO THE PATIENT.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7479161 ↗

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Sources and updates

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