Angiodynamics recalls Soft-Vu Angiographic Catheter models with a defect that may prevent guidewire passage through the hub, risking improper procedures during medical imaging.
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Angiodynamics is recalling Soft-Vu Angiographic Catheters with a manufacturing defect that could prevent the correct guidewire from passing through the catheter hub. This risk may lead to improper medical procedures during angiography.
The catheter hub's inner diameter may be too small for the properly sized guidewire to pass through. This defect could cause the guidewire to get stuck, potentially leading to improper imaging or complications during the procedure.
Healthcare professionals using the Soft-Vu Angiographic Catheter for medical imaging procedures are most at risk. Patients undergoing angiography with these devices could face complications.
Check for the model name 'Soft-Vu CB2 4F X 100CM 038 NB 0SH' or catalog number 10714018. The product was sold in boxes with 5 pouches each.
Verify the model number on the catheter packaging or label to confirm if it matches the recalled items.
Reach out to Angiodynamics directly for guidance on next steps if you have the recalled catheter.
The recalled catheters have a manufacturing defect that may prevent the appropriately sized guidewire from passing through the inner diameter of the hub.
Check the model number and contact Angiodynamics for guidance on next steps.
The defect could lead to improper medical procedures, but the recall does not specify a risk of serious injury in normal use.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-1865-2026 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-1865-2026 from Angiodynamics. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
