Soft-Vu and Accu-Vu 4 FR Angiographic Catheters
In plain language
This recall involves Soft-Vu and Accu-Vu 4 FR Angiographic Catheters sold in Canada. They are being recalled because a manufacturing defect may prevent a guidewire from passing through the catheter. Contact the manufacturer for more information.
What to do
- Stop using the product immediately.
- Contact the manufacturer for additional information.
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Affected products
Specific affected products are listed in the official notice.
Why this matters
Device compatibility issues
Do I have this product?
This recall applies to specific products. Details are listed in the official notice.
Frequently Asked Questions
Why was this product recalled?
Device compatibility issues
What should consumers do?
Stop using the product immediately. Contact the manufacturer for additional information.
Where was the product sold?
This product was sold in Canada. For specific retailers or distribution areas, please check the official recall notice linked on this page.
Is there a health risk?
Yes, there may be a health risk. Device compatibility issues
When was this product recalled?
This product was recalled on March 18, 2026.
Is the AngioDynamics, Inc. brand affected by this recall?
Yes, AngioDynamics, Inc. products are affected by this recall. This recall involves Soft-Vu and Accu-Vu 4 FR Angiographic Catheters sold in Canada. They are being recalled because a manufacturing defect may prevent a guidewire from passing through the catheter. Contact the manufacturer for more information.