Angiodynamics recalls

Angiodynamics has 100 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 29 Apr 2026. 59 are still ongoing. 20 were reported in the last 12 months.

Total recalls100since 2013

Last 12 months20reported

Class I00% of total

Ongoing59latest 29 Apr 2026

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 1 0Feb 1 0 0May 0 0 0Aug 0 0 0Nov 0 0 0Feb 0 20 0May 0 0 0Aug 0 0

Severity split

Class I 0 0%Class II 94 94%Class III 6 6%

Why angiodynamics is recalled

Product types

By year

20262020%
202522%
20243434%
202311%
202222%
202155%
202055%
201966%
201877%
20161111%

Ongoing angiodynamics recalls

59 active

Reported	Class	Recall	Company	Reason	Where
29 Apr 2026Device	CLASS II	Soft-Vu Angiographic Catheter, Headhunter , Non-Braided recalled	Angiodynamics	Device Malfunction	Nationwide
29 Apr 2026Device	CLASS II	Soft -Vu Angiographic Catheter, Kumpe, Non-Braided recalled	Angiodynamics	Device Malfunction	Nationwide
29 Apr 2026Device	CLASS II	Soft-Vu Angiographic Catheter, Cobra , Non-Braided recalled	Angiodynamics	Device Malfunction	Nationwide
29 Apr 2026Device	CLASS II	AccuVu Angiographic Catheter, Omni Flush, Non-Braided recalled	Angiodynamics	Device Malfunction	Nationwide
29 Apr 2026Device	CLASS II	Soft-Vu Angiographic Catheter, Cobra , Non-Braided recalled	Angiodynamics	Device Malfunction	Nationwide
29 Apr 2026Device	CLASS II	Soft-Vu Angiographic Catheter, Sos Omni Selective , Non-Braided recalled	Angiodynamics	Device Malfunction	Nationwide

All angiodynamics recalls, newest first

100 total

Reported	Class	Recall	Company	Reason	Where
29 Apr 2026Device	CLASS II	Soft-Vu Angiographic Catheter, Headhunter , Non-Braided recalled	Angiodynamics	Device Malfunction	Nationwide
29 Apr 2026Device	CLASS II	Soft -Vu Angiographic Catheter, Kumpe, Non-Braided recalled	Angiodynamics	Device Malfunction	Nationwide
29 Apr 2026Device	CLASS II	Soft-Vu Angiographic Catheter, Cobra , Non-Braided recalled	Angiodynamics	Device Malfunction	Nationwide
29 Apr 2026Device	CLASS II	AccuVu Angiographic Catheter, Omni Flush, Non-Braided recalled	Angiodynamics	Device Malfunction	Nationwide
29 Apr 2026Device	CLASS II	Soft-Vu Angiographic Catheter, Cobra , Non-Braided recalled	Angiodynamics	Device Malfunction	Nationwide
29 Apr 2026Device	CLASS II	Soft-Vu Angiographic Catheter, Sos Omni Selective , Non-Braided recalled	Angiodynamics	Device Malfunction	Nationwide
29 Apr 2026Device	CLASS II	Soft-Vu Angiographic Catheter, Straight Art, Non-Braided recalled	Angiodynamics	Device Malfunction	Nationwide
29 Apr 2026Device	CLASS II	Soft-Vu Angiographic Catheter, Pigtail, Non-Braided recalled	Angiodynamics	Device Malfunction	Nationwide
29 Apr 2026Device	CLASS II	Soft-Vu Angiographic Catheter, Omni Flush, Non-Braided recalled	Angiodynamics	Device Malfunction	Nationwide
29 Apr 2026Device	CLASS II	AccuVu Angiographic Catheter, Pigtail, Non-Braided recalled	Angiodynamics	Device Malfunction	Nationwide
29 Apr 2026Device	CLASS II	Soft-Vu Angiographic Catheter, Cobra , Non-Braided recalled	Angiodynamics	Device Malfunction	Nationwide
29 Apr 2026Device	CLASS II	Soft-Vu Angiographic Catheter, Berenstein, Non-Braided recalled	Angiodynamics	Device Malfunction	Nationwide
29 Apr 2026Device	CLASS II	Soft-Vu Angiographic Catheter, Omni Flush, Non-Braided recalled	Angiodynamics	Device Malfunction	Nationwide
29 Apr 2026Device	CLASS II	Soft-Vu Angiographic Catheter, Kumpe, Non-Braided recalled	Angiodynamics	Device Malfunction	Nationwide
29 Apr 2026Device	CLASS II	Soft-Vu Angiographic Catheter, Pigtail, Non-Braided recalled	Angiodynamics	Device Malfunction	Nationwide
29 Apr 2026Device	CLASS II	AccuVu Angiographic Catheter, Omni Flush, Non-Braided recalled	Angiodynamics	Device Malfunction	Nationwide
29 Apr 2026Device	CLASS II	Soft-Vu Angiographic Catheter, Kumpe, Non-Braided recalled	Angiodynamics	Device Malfunction	Nationwide
29 Apr 2026Device	CLASS II	Soft-Vu Angiographic Catheter, Berenstein, Non-Braided recalled	Angiodynamics	Device Malfunction	Nationwide
29 Apr 2026Device	CLASS II	AccuVu Angiographic Catheter, Straight Flush, Non-Braided recalled	Angiodynamics	Device Malfunction	Nationwide
29 Apr 2026Device	CLASS II	Soft-Vu Angiographic Catheter, Kumpe, Non-Braided recalled	Angiodynamics	Device Malfunction	Nationwide
26 Mar 2025Device	CLASS II	IsoLoc Short Profile Prostate Immobilization Treatment recalled	Angiodynamics	Labeling Errors	Nationwide
8 Jan 2025Device	CLASS II	Auryon Laser System 100-120 Vac recalled by Angiodynamics	Angiodynamics	Other	Nationwide
7 Aug 2024Device	CLASS II	Soft-vu Kumpe 5F -Used for patients recalled by Angiodynamics	Angiodynamics	Labeling Errors	Nationwide
7 Aug 2024Device	CLASS II	Soft-vu Kumpe 5F -Used for patients recalled by Angiodynamics	Angiodynamics	Labeling Errors	Nationwide
10 Jul 2024Device	CLASS II	IsoLoc Prostate Immobilization Treatment Balloon Device Kit recalled	Angiodynamics	Labeling Errors	Nationwide
15 May 2024Device	CLASS II	Duramax Stacked Tip Straight Vasc-pak recalled by Angiodynamics	Angiodynamics	Other	VA
15 May 2024Device	CLASS II	Duramax Stacked Tip Str recalled by Angiodynamics	Angiodynamics	Foreign Material	VA
15 May 2024Device	CLASS II	Duraflow 2 Straight Basic Kit, 1 per Bx Pg-Indicated recalled	Angiodynamics	Foreign Material	VA
15 May 2024Device	CLASS II	Duraflow 2 Straight Vasc-pak PG- Indicated for use recalled	Angiodynamics	Foreign Material	VA
15 May 2024Device	CLASS II	Duramax Stacked Tip Str recalled by Angiodynamics	Angiodynamics	Foreign Material	VA

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.