NA 0306131000Recalls & reported problems
Stryker Corporation · Match-Ground Bevel Tip Introduction Needle · Class 1
- 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 04546540434319), received between Jan 14, 2026 and Jan 14, 2026 — classified as 1 injury.
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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Pain1
- Unspecified Infection1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 14, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT DURING A CEMENTOPLASTY THAT INVOLVED STRYKER DEVICES THAT THE PATIENT SUFFERED AN INFECTION POST PROCEDURE. IT SHOULD BE NOTED THAT THERE WERE NO ISSUES WITH ANY OF THE DEVICES USED. AT THE TIME OF THE PROCEDURE THERE WERE NO PATIENT ISSUES REPORTED. THE PATIENT WAS HOSPITALIZED IN (B)(6) 2025 WITH A BACTERIAL INFECTION. WE ARE TRYING TO GATHER MORE INFORMATION OF WHAT OCCURRED DURING THAT TIME IN THE HOSPITAL.
Patient problems: Pain; Unspecified Infection
MAUDE report 24070027 ↗
Other Injector, vertebroplasty (does not contain cement) devices
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- DFINE® 00884450374375Merit Medical Systems, Inc. · Injector, vertebroplasty (does not contain cement)1 recall0 reports
- PCD 0506485000Stryker Corporation · Injector, vertebroplasty (does not contain cement)1 recall0 reports
- StabiliT TOUCH™ Syringe 00884450662144Merit Medical Systems, Inc. · Injector, vertebroplasty (does not contain cement)1 recall0 reports
- DFINE® 00884450374399Merit Medical Systems, Inc. · Injector, vertebroplasty (does not contain cement)1 recall0 reports
- VertePort 0306511000Stryker Corporation · Injector, vertebroplasty (does not contain cement)1 recall0 reports
- iVAS 0306330000Stryker Corporation · Injector, vertebroplasty (does not contain cement)41 reports
- VERTECEM II 03.702.215SSynthes GmbH · Injector, vertebroplasty (does not contain cement)22 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.