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XIA II 03820133Recalls & reported problems

Stryker Corporation · LONG OFFSET CONNECTOR NEUTRAL · Class 2 · Implant

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04546540468956), received between Jun 23, 2020 and Jun 23, 2020 — classified as 1 injury.

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

  • Migration1

Patient problems

  • Pain1

Recent adverse event reports

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

  • InjuryJun 23, 2020Migration; Migration

    IT WAS REPORTED THAT AN UNKNOWN ROD BROKE BETWEEN LEFT L4 AND L5 POST-OPERATIVELY. AS A RESULT, THE ILIAC SCREW AND OFFSET CONNECTOR ON THE RIGHT SIDE OF THE HEAD WERE DISPLACED, CAUSING PAIN. REVISION SURGERY WAS PERFORMED. THIS REPORT REPRESENTS THE CONNECTOR.

    Patient problems: Pain

    MAUDE report 10186433 ↗

Other APPLIANCE, FIXATION, SPINAL INTERLAMINAL devices

All APPLIANCE, FIXATION, SPINAL INTERLAMINAL devices →

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