Angiodynamics, Inc. 2026-04-29 Health serious FDA
Health · FDA · Recall #FDA-Z-1863-2026
Soft-Vu Angiographic Catheter, Berenstein, Non-Braided; SOFT-VU BER 4F X 100CM 038 NB… Recall
Issued April 29, 2026 · Angiodynamics, Inc.
In April 2026, Angiodynamics, Inc. recalled the Soft-Vu Angiographic Catheter, Berenstein, Non-Braided; SOFT-VU BER 4F X 100CM 038 NB…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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 you should do
- 1 Stop using Soft-Vu Angiographic Catheter, Berenstein, Non-Braided; SOFT-VU BER 4F X 100CM 038 NB… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Angiodynamics, Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Angiodynamics, Inc.
- Category
- Health
- Recall date
- April 29, 2026
- Units affected
- Not reported
- Sold at
- Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, China, Chile, Curacao, Czech Republic, Germ
- Recall number
- FDA-Z-1863-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Angiodynamics, Inc. has 9 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 356th Health recall we've logged in 2026.