Angiodynamics recalls AccuVu Angiographic Catheters with a defect that may prevent guidewires from passing through the hub, risking procedure complications. Affected units include specific model numbers and lot codes.
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 certain AccuVu Angiographic Catheters due to a defect that may prevent the correct size guidewire from passing through the catheter hub. This could lead to complications during medical procedures if the catheter is used without proper guidance.
The catheter hub's inner diameter may be too small for the appropriate guidewire size, preventing it from passing through. This could cause the catheter to become stuck during medical procedures, potentially leading to complications like bleeding or tissue damage.
Healthcare professionals using the catheters for medical procedures are most at risk. Patients receiving these catheters during procedures may face complications if the defect causes improper guidewire passage.
Check for the model number ACCU-VU STR FL 4F X 100CM 035 NB 6SH 10 R/O 6@1CM 4@5CM. The product box has a catalog number 13709604 and lot number A2825044.
Verify the model number and lot number on the product box and pouch to confirm if it 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, which could cause complications during medical procedures.
The recall record does not specify a remedy, so contact Angiodynamics directly for guidance on next steps.
Check for the model number ACCU-VU STR FL 4F X 100CM 035 NB 6SH 10 R/O 6@1CM 4@5CM and lot number A2825044 on the product box and pouch.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-1873-2026 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-1873-2026 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.
