Angiodynamics recalls Soft-Vu Angiographic Catheter (Kumpe, Non-Braided) due to a defect preventing proper 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 Soft-Vu Angiographic Catheters with a specific model number because a manufacturing defect might prevent the correct size guidewire from passing through the catheter hub. This could cause complications during medical procedures if the catheter is used improperly.
The catheter hub's inner diameter may be too small for the appropriate guidewire size, which could lead to complications like blockages or improper catheter placement during medical procedures.
Healthcare professionals using the Soft-Vu Angiographic Catheter for medical procedures are most at risk if the defect prevents proper guidewire passage during procedures.
Check for the model: SOFT-VU KMP 4F X 100CM 038 NB 0SH with catalog number 10714021. The product was sold with specific lot numbers: A2525059, A3725003, and A3725004.
Verify the model number and catalog number on the product packaging to confirm if it 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 official recall notice does not specify a remedy or action steps for affected products.
Check for the model: SOFT-VU KMP 4F X 100CM 038 NB 0SH with catalog number 10714021 and lot numbers A2525059, A3725003, or A3725004.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-1866-2026 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-1866-2026 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.
