Angiodynamics recalls Soft-Vu Angiographic Catheter (SOFT-VU PT 4F X 65CM 038 NB 10SH) due to a defect preventing guidewire passage. This could cause 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 may prevent the correct guidewire from passing through the catheter hub. This could lead to 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 cause the catheter to become stuck during medical procedures, potentially leading to complications.
Healthcare professionals who use 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 PT 4F X 65CM 038 NB 10SH with Catalog Number 10714002. The product was sold with Lot Numbers A2525060, A2525061, A3625006, or A3625007.
Verify the model number and lot numbers listed in the recall notice 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 remedy is applied.
The recall does not specify a remedy, so contact Angiodynamics directly for guidance on next steps.
Check for the model SOFT-VU PT 4F X 65CM 038 NB 10SH with Catalog Number 10714002 and Lot Numbers A2525060, A2525061, A3625006, or A3625007.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-1859-2026 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-1859-2026 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.
