Reported Apr 29, 2026 · Ongoing
Soft-Vu Angiographic Catheter, Cobra (2), Non-Braided; SOFT-VU CB2 4F X 100CM 038 NB 0SH; Catalog No.: 10714018;…
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 CatheterCobra (2)Non-BraidedSOFT-VU CB2 4F X 100CM 038 NB 0SHCatalog No.: 10714018Product/UPN No.: H787107140185 (Box)H787107140180 (Pouch)
- Box Quantity5 pouches
- Lot codes and dates
SOFT-VU CB2 4F X 100CM 038 NB 0SHCatalog No.: 10714018Product/UPN No.: H787107140185 (Box)H787107140180 (Pouch)
- UDI-DI
25051684007938(Box)15051684007931(Pouch)Lot No.: A2825145
- Amount recalled
- 210 units (42 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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