FDAMarch 3, 2026device

AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 2 R/O Markers; ACCU-VU OF 4F X 70CM 035 NB 6SH 2 R/O 2CM; Catalog No.: 13709005; Product/UPN No.: H787137090055 (Box), H787137090050 (Pouch); Box Quantity: 5 pouches;

Official recall recorded by the U.S. Food & Drug Administration.

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.

What to do

FDA enforcement status: Ongoing

Brands named

angiodynamics

UPCs

2505168400571215051684005715

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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