VertePort 0306511000Recalls & reported problems
Stryker Corporation · Cement Cannula · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier.
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.
Recalls naming this device
- Nov 9, 2017Terminated
Lack of sterility assurance as bioburden levels were found to be higher than internal acceptable rates.
Z-1247-2018 · Root cause: Environmental control · FDA record ↗
Other Injector, vertebroplasty (does not contain cement) devices
- AVAflex 1025011500Stryker Corporation · Injector, vertebroplasty (does not contain cement)1 recall9 reports
- 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
- 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
- AVAflex 1025011000Stryker Corporation · Injector, vertebroplasty (does not contain cement)11 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page