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VertePort 0306410000Recalls & reported problems

Stryker Corporation · Cement Cannula for Kit · Class 1

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613154511051), received between Nov 21, 2018 and May 8, 2019 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Contamination /Decontamination 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

  • Contamination /Decontamination Problem1
  • Delivered as Unsterile Product1
  • Unsealed Device Packaging1

Patient problems

  • No Patient Involvement2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMay 8, 2019Delivered as Unsterile Product; Delivered as Unsterile Product

    IT WAS REPORTED THAT THERE WAS A HAIR IN THE STERILE PACKAGING. THERE WAS NO ASSOCIATED PROCEDURE.

    Patient problems: No Patient Involvement

    MAUDE report 8591244 ↗
  • MalfunctionNov 21, 2018Unsealed Device Packaging; Contamination /Decontamination Problem; Unsealed Device Packaging; Contamination /Decontamination Problem

    IT WAS REPORTED THAT THE STERILE PACKAGING TORE DOWN SIDEWAYS UPON OPENING THE DEVICE AND CONTAMINATED THE PRODUCT. THERE WAS NO ASSOCIATED PROCEDURE AND THEREFORE, NO PATIENT INVOLVEMENT.

    Patient problems: No Patient Involvement

    MAUDE report 8096209 ↗

Other Injector, vertebroplasty (does not contain cement) devices

All Injector, vertebroplasty (does not contain cement) devices →

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