Angiodynamics recalls AccuVu Angiographic Catheters with a defect that may prevent guidewires from passing through the hub, risking procedure complications. Affected units have specific model 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 certain AccuVu Angiographic Catheters due to a defect that may prevent the properly sized guidewire from passing through the catheter hub. This 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 the guidewire to get stuck, potentially leading to procedure complications or the need for additional interventions.
Healthcare professionals who use these catheters during medical procedures are most at risk. Patients receiving procedures with the affected catheters could face complications.
Check for the model number ACCU-VU OF 4F X 70CM 035 NB 6SH 21 R/O 1CM. Lot numbers A3025039 or A3225033 are also associated with the affected units.
Verify the model number and lot number on the catheter packaging to determine if it is affected.
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter of the catheter hub.
The recall does not specify a remedy, so check the product details to see if it is affected and contact the manufacturer for further instructions.
Look for the model number ACCU-VU OF 4F X 70CM 035 NB 6SH 21 R/O 1CM and lot numbers A3025039 or A3225033.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-1874-2026 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-1874-2026 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.
