Angiodynamics recalls Soft-Vu Angiographic Catheter (SOFT-VU OF 4F X 65CM 035 NB 6SH) due to a defect preventing guidewire passage through the catheter hub. This could lead to complications during medical procedures.
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 a specific type of angiographic catheter because a manufacturing defect might prevent the correct guidewire from passing through the catheter hub. This could cause complications during medical procedures if the catheter is used improperly.
The catheter hub has a defect that may prevent the properly sized guidewire from passing through its inner diameter. This could lead to complications during medical procedures if the catheter is used without the correct guidewire.
Healthcare professionals using this catheter for medical imaging procedures are most at risk. Patients receiving these procedures may be affected if the catheter is used incorrectly.
Check for the model SOFT-VU OF 4F X 65CM 035 NB 6SH with catalog number 10732301. The product was sold with lot numbers A2825022, A3025035, or A3025037.
Identify the model number and lot numbers to confirm if your catheter is affected.
The recall indicates a potential defect that could prevent guidewire passage, so it is not recommended for use until the issue is resolved.
Check the model and lot numbers to see if it is affected; contact Angiodynamics for further instructions.
Look for the model SOFT-VU OF 4F X 65CM 035 NB 6SH with catalog number 10732301 and lot numbers A2825022, A3025035, or A3025037.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-1870-2026 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-1870-2026 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.
