Angiodynamics, Inc.

Frequent Recalls

Recalls

Units Recalled

Injuries

Deaths

2026-04-29 to 2026-04-29

Date	Source	Product	Brand	Severity	Units
2026-04-29	FDA Device	FDA Recall: AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 2 R/O Markers; ACCU-VU OF 4F X 70CM 035	Angiodynamics, Inc.	Class II	N/A
2026-04-29	FDA Device	FDA Recall: Soft-Vu Angiographic Catheter, Omni Flush, Non-Braided; SOFT-VU OF 4F X 65CM 038 NB 6SH; Catalog N	Angiodynamics, Inc.	Class II	N/A
2026-04-29	FDA Device	FDA Recall: Soft-Vu Angiographic Catheter, Berenstein, Non-Braided; SOFT-VU BER 4F X 100CM 038 NB 0SH; Catalog	Angiodynamics, Inc.	Class II	N/A
2026-04-29	FDA Device	FDA Recall: Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 65CM 038 NB 0SH; Catalog No.:	Angiodynamics, Inc.	Class II	N/A
2026-04-29	FDA Device	FDA Recall: Soft-Vu Angiographic Catheter, Pigtail, Non-Braided; SOFT-VU PT 4F X 65CM 038 NB 10SH; Catalog No.	Angiodynamics, Inc.	Class II	N/A
2026-04-29	FDA Device	FDA Recall: Soft-Vu Angiographic Catheter, Straight Art, Non-Braided; SOFT-VU STR ART 4F X 65CM 035 NB 0SH; Ca	Angiodynamics, Inc.	Class II	N/A
2026-04-29	FDA Device	FDA Recall: Soft-Vu Angiographic Catheter, Sos Omni Selective (1), Non-Braided; SOFT-VU SO1 4F X 80CM 038 NB 0S	Angiodynamics, Inc.	Class II	N/A
2026-04-29	FDA Device	FDA Recall: Soft-Vu Angiographic Catheter, Headhunter (1), Non-Braided; SOFT-VU HH1 4F X 100CM 038 NB 0SH; Cat	Angiodynamics, Inc.	Class II	N/A
2026-04-29	FDA Device	FDA Recall: Soft-Vu Angiographic Catheter, Berenstein, Non-Braided; SOFT-VU BER 4F X 65CM 038 NB 0SH; Catalog	Angiodynamics, Inc.	Class II	N/A
2026-04-29	FDA Device	FDA Recall: AccuVu Angiographic Catheter, Pigtail, Non-Braided, With 21 R/O Markers; ACCU-VU PT 4F X 70CM 035 N	Angiodynamics, Inc.	Class II	N/A
2026-04-29	FDA Device	FDA Recall: Soft-Vu Angiographic Catheter, Omni Flush, Non-Braided; SOFT-VU OF 4F X 65CM 035 NB 6SH; Catalog N	Angiodynamics, Inc.	Class II	N/A
2026-04-29	FDA Device	FDA Recall: Soft-Vu Angiographic Catheter, Pigtail, Non-Braided; SOFT-VU PT 4F X 100CM 035 NB 10SH; Catalog No	Angiodynamics, Inc.	Class II	N/A
2026-04-29	FDA Device	FDA Recall: AccuVu Angiographic Catheter, Straight Flush, Non-Braided, With 10 R/O Markers; ACCU-VU STR FL 4F X	Angiodynamics, Inc.	Class II	N/A
2026-04-29	FDA Device	FDA Recall: Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 100CM 038 NB 0SH; Catalog No.:	Angiodynamics, Inc.	Class II	N/A
2026-04-29	FDA Device	FDA Recall: Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 40CM 035 NB 0SH; Catalog No.:	Angiodynamics, Inc.	Class II	N/A
2026-04-29	FDA Device	FDA Recall: Soft-Vu Angiographic Catheter, Cobra (2), Non-Braided; SOFT-VU CB2 4F X 100CM 038 NB 0SH; Catalog	Angiodynamics, Inc.	Class II	N/A
2026-04-29	FDA Device	FDA Recall: AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 21 R/O Markers; ACCU-VU OF 4F X 70CM 03	Angiodynamics, Inc.	Class II	N/A
2026-04-29	FDA Device	FDA Recall: Soft-Vu Angiographic Catheter, Cobra (2), Non-Braided; SOFT-VU CB2 4F X 65CM 038 NB 0SH; Catalog N	Angiodynamics, Inc.	Class II	N/A
2026-04-29	FDA Device	FDA Recall: Soft -Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 40CM 038 NB 0SH; Catalog No.:	Angiodynamics, Inc.	Class II	N/A
2026-04-29	FDA Device	FDA Recall: Soft-Vu Angiographic Catheter, Cobra (1), Non-Braided; SOFT-VU CB1 4F X 100CM 038 NB 0SH; Catalog	Angiodynamics, Inc.	Class II	N/A