AxiumTMRecalls & reported problems across all models
Micro Therapeutics, Inc. · 139 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
AxiumTM models — page 2
139 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- AxiumTM FC-3-10-3DDEVICE, NEUROVASCULAR EMBOLIZATION1 report
- AxiumTM FC-4-8-3DDevice, Vascular, for Promoting Embolization1 report
- AxiumTM FC-4-12-3DDevice, Vascular, for Promoting Embolization1 report
- AxiumTM FC-5-10-3DDEVICE, NEUROVASCULAR EMBOLIZATION1 report
- AxiumTM FC-5-15-3DDevice, Vascular, for Promoting Embolization1 report
- AxiumTM FC-5-20-3DDEVICE, NEUROVASCULAR EMBOLIZATION1 report
- AxiumTM FC-7-20-3DDEVICE, NEUROVASCULAR EMBOLIZATION1 report
- AxiumTM FC-8-15-3DDevice, Vascular, for Promoting Embolization1 report
- AxiumTM QC-2-1-HELIXDevice, Vascular, for Promoting Embolization1 report
- AxiumTM QC-2-3-HELIXDevice, Vascular, for Promoting Embolization1 report
- AxiumTM QC-4-8-HELIXDevice, Vascular, for Promoting Embolization1 report
- AxiumTM QC-5-15-HELIXDevice, Vascular, for Promoting Embolization1 report
- AxiumTM QC-5-20-HELIXDevice, Vascular, for Promoting Embolization1 report
- AxiumTM QC-6-20-HELIXDevice, Vascular, for Promoting Embolization1 report
- AxiumTM QC-7-20-HELIXDevice, Vascular, for Promoting Embolization1 report
- AxiumTM QC-7-30-HELIXDevice, Vascular, for Promoting Embolization1 report
- AxiumTM QC-8-30-HELIXDevice, Vascular, for Promoting Embolization1 report
- AxiumTM QC-9-20-HELIXDEVICE, NEUROVASCULAR EMBOLIZATION1 report
- AxiumTM QC-10-30-HELIXDevice, Vascular, for Promoting Embolization1 report
- AxiumTM QC-18-40-HELIXDevice, Vascular, for Promoting Embolization1 report
- AxiumTM QC-2-2-3DDevice, Vascular, for Promoting Embolization1 report
- AxiumTM QC-2.5-6-3DDEVICE, NEUROVASCULAR EMBOLIZATION1 report
- AxiumTM QC-3.5-12-3DDEVICE, NEUROVASCULAR EMBOLIZATION1 report
- AxiumTM QC-4-10-3DDevice, Vascular, for Promoting Embolization1 report
- AxiumTM QC-5-10-3DDevice, Vascular, for Promoting Embolization1 report
- AxiumTM QC-6-10-3DDevice, Vascular, for Promoting Embolization1 report
- AxiumTM QC-9-30-3DDEVICE, NEUROVASCULAR EMBOLIZATION1 report
- AxiumTM QC-18-40-3DDevice, Vascular, for Promoting Embolization1 report
- AxiumTM QC-22-50-3DDevice, Vascular, for Promoting Embolization1 report
- AxiumTM QC-25-50-3DDevice, Vascular, for Promoting Embolization1 report
- AxiumTM NC-2-4-HELIXDEVICE, NEUROVASCULAR EMBOLIZATION1 report
- AxiumTM PC-2-2-HELIXDEVICE, NEUROVASCULAR EMBOLIZATION1 report
- AxiumTM PC-4-8-HELIXDevice, Vascular, for Promoting Embolization1 report
- AxiumTM PC-9-30-HELIXDevice, Vascular, for Promoting Embolization1 report
- AxiumTM PC-2-6-3DDEVICE, NEUROVASCULAR EMBOLIZATION1 report
- AxiumTM PC-3-6-3DDEVICE, NEUROVASCULAR EMBOLIZATION1 report
- AxiumTM PC-5-15-3DDevice, Vascular, for Promoting Embolization1 report
- AxiumTM PC-7-20-3DDevice, Vascular, for Promoting Embolization1 report
- AxiumTM PC-8-30-3DDevice, Vascular, for Promoting Embolization1 report
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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