Stereotaxis Inc Cronus Endovascular Guidewire, Length 210 cm (full coat), Diameter 0.014 inch, Part Number 001-001096-1 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Cronus Endovascular Guidewire, Length 210 cm (full coat), Diameter 0.014 inch, Part Number 001-001096-1
Brand
Stereotaxis Inc
Lot Codes / Batch Numbers
Lots 0206-4004, 0207-4005, 0301-4015, 0301-4016, and 0304-4020
Products Sold
Lots 0206-4004, 0207-4005, 0301-4015, 0301-4016, and 0304-4020
Stereotaxis Inc is recalling Cronus Endovascular Guidewire, Length 210 cm (full coat), Diameter 0.014 inch, Part Number 001-00109 due to The magnet at the end of the guidewire could break off.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The magnet at the end of the guidewire could break off.
Recommended Action
Per FDA guidance
Consignees were sent a notice dated January 27, 2004. The notice requested that consignees stop using the product and stated that a firm representative would contact the consignees. The firm''s representatives have retrieved all of the product at the consignees.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026