Angiodynamics recalls Soft-Vu Angiographic Catheter models with a defect that may prevent guidewire passage through the catheter hub, risking improper procedure. Affected units include specific model numbers and catalog codes.
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 Catheter models that have a defect preventing properly sized guidewires from passing through the catheter hub. This could lead to improper medical procedures if the catheter is used without the guidewire being able to move freely.
The defect may cause the catheter hub to be too small for the guidewire to pass through, which could lead to improper placement of the catheter during medical procedures. This might result in ineffective treatment or complications if the catheter is not properly positioned.
Healthcare professionals using the Soft-Vu Angiographic Catheter for medical procedures are most at risk if the defect prevents guidewire passage during treatment.
Check for the model number SOFT-VU CB1 4F X 100CM 038 NB 0SH, catalog number 10714017, or product code H787107140175 (box) and H787107140170 (pouch). The recall includes specific lot numbers and UDI-DI codes.
Verify the model number, catalog number, and product codes to confirm if your catheter is affected.
The affected devices contain a manufacturing defect that may prevent the appropriately sized guidewire from passing through the inner diameter of the catheter hub.
The affected models include SOFT-VU CB1 4F X 100CM 038 NB 0SH with catalog number 10714017.
Check for the model number SOFT-VU CB1 4F X 100CM 038 NB 0SH, catalog number 10714017, or product codes H787107140175 (box) and H787107140170 (pouch).
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-1864-2026 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-1864-2026 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.
