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Medium risk Medical DevicesClass II

AccuVu Angiographic Catheter Recall

AccuVu Angiographic Catheter, Straight Flush, Non-Braided, With 10 R/O Markers; ACCU-VU STR FL 4F X 100CM 035 NB 6SH 10 R/O 6@1CM 4@5CM; Cat

Updated March 3, 2026

AccuVu Angiographic Catheters with certain catalog and product numbers contain a manufacturing defect that may prevent a guidewire from passing through the catheter hub, potentially delaying or complicating medical procedures.

Is the Angiodynamics, Inc. recalled? Yes. This product was recalled by FDA on March 3, 2026. Details below.

What is recalled

AccuVu Angiographic Catheter, Straight Flush, Non-Braided, With 10 R/O Markers (ACCU-VU STR FL 4F X 100CM 035 NB 6SH 10 R/O 6@1CM 4@5CM). Catalog No. 13709604. Product/UPN No. H787137096045 (Box) and H787137096040 (Pouch).

Am I affected

You are affected if you have this catheter in your facility and the box or pouch is labeled with UPN H787137096045 or H787137096040, or catalog number 13709604.

What to do right now

Stop using these catheters immediately and contact Angiodynamics, Inc. directly for instructions on return or replacement of the affected units.

The hazard

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.

Brands affected

Angiodynamics, Inc.
Source
FDA
Category
Medical Devices
Recall ID
fda-Z-1873-2026
Classification
Class II
Recalled
March 3, 2026
Read the official notice

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