Angiodynamics recalls Soft-Vu Angiographic Catheter models with a defect that may prevent guidewire passage through the 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 may prevent a properly sized guidewire from passing through the catheter hub. This defect could lead to improper medical procedures if the catheter is used without the guidewire fitting correctly.
The catheter hub's inner diameter may be too small for the intended guidewire size, causing the guidewire to get stuck. This could lead to complications during medical procedures if the catheter is used without the guidewire fitting correctly.
Healthcare professionals using the Soft-Vu Angiographic Catheter for medical procedures are most at risk if the device is used without the guidewire passing through the hub.
Check for the model number SOFT-VU CB2 4F X 65CM 038 NB 0SH, catalog number 10714011, or product codes H787107140115 (box) and H787107140110 (pouch). The recall includes specific lot numbers A3025038 and A3025051.
Identify the model number, catalog number, or product codes to confirm if your catheter is affected.
The affected devices have 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 CB2 4F X 65CM 038 NB 0SH with catalog number 10714011.
Check for the model number SOFT-VU CB2 4F X 65CM 038 NB 0SH, catalog number 10714011, or product codes H787107140115 (box) and H787107140110 (pouch).
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-1861-2026 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-1861-2026 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.
