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DIAPASON 665140Recalls & reported problems

Stryker Corporation · ROD · 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 04546540320384), received between Mar 19, 2020 and Mar 19, 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

  • Injury1

Recent adverse event reports

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

  • InjuryMar 19, 2020Migration; Migration

    IT WAS DISCOVERED VIA X-RAY THAT A 120MM AND 140MM DIAPASON ROD DISENGAGED FROM THE RESPECTED CROSS CONNECTOR 2 YEARS POST-OPERATIVELY. REVISION SURGERY WAS CONDUCTED WHERE REINFORCEMENT AND BONE GRAFTING WAS PERFORMED TO DISPERSE THE MECHANICAL LOAD. THE DIAPASON ROD REMAINS IN THE PATIENT. THIS RECORD REPRESENTS THE 140MM DIAPASON ROD.

    Patient problems: Injury

    MAUDE report 9858129 ↗

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.