Stereotaxis Inc
Saint Louis, MO
This page shows every FDA and USDA recall linked to Stereotaxis Inc. Each entry includes the product involved, when the recall happened, and how serious it was. If a company has had multiple recalls over the years, you can see the full history here in one place — including whether any were Class I, which is the most serious type.
7
Total Recalls
2004
First Recall
2020
Most Recent
Niobe ES System, Models 001-006000-1 and 001-006100-1
Sep 21, 2020
· Device
Terminated
Cronus Endovascular Guidewire, Length 210 cm (full coat), Diameter 0.014 inch, Part Number 001-001096-1
Jul 20, 2004
· Device
Terminated
Cronus Endovascular Guidewire, Length 300 cm (partial coat), Diameter 0.014 inch, Part Number 001-001096-4
Jul 20, 2004
· Device
Terminated
Floppy Cronus Endovascular Guidewire, Length 180 cm (partial coat), Diameter 0.014 inch, Part Number 001-00123...
Jul 20, 2004
· Device
Terminated
Cronus-1 Endovascular Guidewire, Length 210 cm (full coat), Diameter 0.014 inch, Part Number 001-001263-1
Jul 20, 2004
· Device
Terminated
Floppy Cronus Endovascular Guidewire, Length 300 cm (partial coat), Diameter 0.014 inch, Part Number 001-00123...
Jul 20, 2004
· Device
Terminated
Cronus Endovascular Guidewire, Length 210 cm (partial coat), Diameter 0.014 inch, Part Number 001-001096-3
Jul 20, 2004
· Device
Terminated