Angiodynamics recalls Soft-Vu Angiographic Catheter models with a defect that may prevent guidewire passage through the hub, risking procedure complications.
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 properly sized guidewires from passing through the catheter hub. This could lead to procedure complications if the catheter is used in medical procedures.
The catheter hub has a manufacturing defect that may prevent the appropriately sized guidewire from passing through its inner diameter. This could cause the catheter to become stuck during medical procedures, potentially leading to complications.
Medical professionals using the Soft-Vu Angiographic Catheter for procedures are most at risk. The affected models are used in hospital settings for imaging procedures.
Check for the model name 'SOFT-VU PT 4F X 100CM 035 NB 10SH' or catalog number 10707103. The product was sold with box quantity 10 units.
Verify the model number and catalog number on the product packaging to confirm if it 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 recall record does not specify a remedy, so contact Angiodynamics directly for guidance.
Check for the model name 'SOFT-VU PT 4F X 100CM 035 NB 10SH' or catalog number 10707103 on the packaging.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-1856-2026 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-1856-2026 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.
