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NA 340710Recalls & reported problems

Stryker GmbH · Cortex Screw S.T. · Class 2 · Implant

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
4
Deaths reported
0
Injuries reported
4
Recalls naming it
0

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 07613327080896), received between Dec 23, 2019 and Dec 23, 2019 — classified as 4 injuries.

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 16, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem4

Patient problems

  • Itching Sensation4

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

  • InjuryDec 23, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    THE MOTHER OF A PATIENT CONTACTED STRYKER BY PHONE. HER DAUGHTER HAD AN ALLERGIC REACTION (ITCHING) AFTER A SURGERY WITH STRYKER PRODUCTS. AN APPOINTMENT WITH THE DERMATOLOGIST HAS ALREADY BEEN MADE. ADDITIONALLY REPORTED: THE ITCHING INITIALLY OCCURRED ONLY ON THE LEGS, BUT NOW ON THE WHOLE BODY."

    Patient problems: Itching Sensation

    MAUDE report 9513197 ↗
  • InjuryDec 23, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    THE MOTHER OF A PATIENT CONTACTED STRYKER BY PHONE. HER DAUGHTER HAD AN ALLERGIC REACTION (ITCHING) AFTER A SURGERY WITH STRYKER PRODUCTS. AN APPOINTMENT WITH THE DERMATOLOGIST HAS ALREADY BEEN MADE. ADDITIONALLY REPORTED: THE ITCHING INITIALLY OCCURRED ONLY ON THE LEGS, BUT NOW ON THE WHOLE BODY."

    Patient problems: Itching Sensation

    MAUDE report 9513196 ↗
  • InjuryDec 23, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED, THE MOTHER OF A PATIENT CONTACTED STRYKER BY PHONE. HER DAUGHTER HAD AN ALLERGIC REACTION (ITCHING) AFTER A SURGERY WITH STRYKER PRODUCTS. AN APPOINTMENT WITH THE DERMATOLOGIST HAS ALREADY BEEN MADE. ADDITIONALLY REPORTED: THE ITCHING INITIALLY OCCURRED ONLY ON THE LEGS, BUT NOW ON THE WHOLE BODY."

    Patient problems: Itching Sensation

    MAUDE report 9513195 ↗
  • InjuryDec 23, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    THE MOTHER OF A PATIENT CONTACTED STRYKER BY PHONE. HER DAUGHTER HAD AN ALLERGIC REACTION (ITCHING) AFTER A SURGERY WITH STRYKER PRODUCTS. AN APPOINTMENT WITH THE DERMATOLOGIST HAS ALREADY BEEN MADE. ADDITIONALLY REPORTED: THE ITCHING INITIALLY OCCURRED ONLY ON THE LEGS, BUT NOW ON THE WHOLE BODY."

    Patient problems: Itching Sensation

    MAUDE report 9513186 ↗

Other PLATE, FIXATION, BONE devices

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Sources and updates

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