Angiodynamics recalls Soft-Vu Angiographic Catheters with a defect that may prevent guidewires from passing through the hub, risking procedure complications. Affected models include SOFT-VU KMP 4F X 40CM 035 NB 0SH with specific catalog and lot numbers.
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 that may prevent properly sized guidewires from passing through the catheter hub. This defect could lead to complications during medical procedures if the catheter is used without the guidewire being able to pass through.
The catheter hub has a manufacturing defect that may prevent the appropriately sized guidewire from passing through its inner diameter. This could cause complications during medical procedures if the catheter is used without the guidewire being able to pass through the hub.
Healthcare professionals using the Soft-Vu Angiographic Catheter for medical procedures are most at risk. Patients receiving these procedures may be affected if the catheter is used incorrectly.
Check for the model SOFT-VU KMP 4F X 40CM 035 NB 0SH with catalog number 10734301. The product was sold with specific lot numbers: A2825021, A2825129, A3325027, A3425027, A3525014, A3825095.
Verify the model number and lot numbers listed in the recall notice to confirm if your catheter is affected.
The affected catheters have a manufacturing defect that may prevent the appropriately sized guidewire from passing through the inner diameter of the hub.
The recall notice does not specify a remedy, so check the product details to confirm if your catheter is affected.
Look for the model SOFT-VU KMP 4F X 40CM 035 NB 0SH with catalog number 10734301 and lot numbers A2825021, A2825129, A3325027, A3425027, A3525014, or A3825095.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-1871-2026 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-1871-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
