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XIA 4 5 481321060Recalls & reported problems

Stryker Corporation · TITANIUM PREBENT AND PRECUT ROD WITHOUT HEX · Class 2 · Implant

All models of XIA 4 5 (32)

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 07613327003253), received between May 9, 2019 and May 9, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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

  • Device Dislodged or Dislocated1
  • Unintended Movement1

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.

  • MalfunctionMay 9, 2019Device Dislodged or Dislocated; Unintended Movement; Unintended Movement

    IT WAS REPORTED A PATIENT COMPLAINED OF CLICKING IN HIS BACK; X-RAY SHOWED THE ROD PULLED OUT OF BOTTOM SCREW POST OPERATIVELY. NO ADVERSE EVENT TO THE PATIENT AND NO PLANS FOR A REVISION AT THIS TIME.

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

    MAUDE report 8597938 ↗

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Sources and updates

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