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ES2 SPINAL SYSTEM 482804435Recalls & reported problems

Stryker Corporation · LONG BLADE CANNULATED SCREW · Class 2 · Implant

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 07613327002300), received between Feb 24, 2016 and Feb 24, 2016 — classified as 1 malfunction.

The most frequently reported specific device problem is “Connection Problem” (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

  • Adverse Event Without Identified Device or Use Problem1
  • Connection Problem1

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.

  • MalfunctionFeb 24, 2016Adverse Event Without Identified Device or Use Problem; Connection Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT DURING SURGERY, THE SCREW DID NOT BE ATTACHED TO THE DRIVER SMOOTHLY. THE REDUCTION THREAD OF THE SCREW SEEMED TO BE DEFORMED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 5458130 ↗

Other Orthosis, spondylolisthesis spinal fixation devices

All Orthosis, spondylolisthesis spinal fixation devices →

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