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. The most frequent reason is device malfunction.

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

0Oct '24 0 0 1Jan '25 0 1 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 20Apr 0 0 0Jul 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

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.