Reported Apr 29, 2026 · Ongoing
Soft-Vu Angiographic Catheter, Omni Flush, Non-Braided; SOFT-VU OF 4F X 65CM 038 NB 6SH; Catalog No.: 10714001;…
Angiodynamics, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Angiodynamics, Inc. · 603 Queensbury Ave · Queensbury, NY · 12804-7619
Is this the product you have?
- Soft-Vu Angiographic Catheter, Omni Flush, Non-Braided; SOFT-VU OF 4F X 65CM 038 NB 6SH; Catalog No.: 10714001; Product/UPN No.: H787107140015 (Box), H787107140010 (Pouch)
- Box Quantity10 pouches
- Lot codes and dates
5 of 5 products
Products covered by this recall Model / number Barcodes Product as published — SOFT-VU OF 4F X 65CM 038 NB 6SH 10714001— — Product/UPN No.: H787107140015 (Box), H787107140010 (Pouch) — 2505168400777815051684007771UDI-DI: 25051684007778(Box), 15051684007771(Pouch) — Lot No.: A2425078, A3325036, A3525030, A3525031, A3725102 - Amount recalled
- 1550 units (155 boxes)
This recall covers 20 products
The agency filed one notice per product. You are reading one of them; the other 19 are below.
7 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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