Angiodynamics, Inc. recalls

22 recalls on record · latest: March 3, 2026

Official U.S. recall history for Angiodynamics, Inc., compiled from official government records.

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Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter, Headhunter (1), Non-Braided; SOFT-VU HH1 4F X 100CM 038 NB 0SH; Catalog No.: 10714040; P…

March 3, 2026 · Medical device recalls Moderate risk The affected devices contain a manufacturing defect which may prevent the appro…

Angiodynamics, Inc. recalls Soft -Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 40CM 038 NB 0SH; Catalog No.: 10710013; Product/UP…

March 3, 2026 · Medical device recalls Moderate risk The affected devices contain a manufacturing defect which may prevent the appro…

Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter, Cobra (2), Non-Braided; SOFT-VU CB2 4F X 65CM 038 NB 0SH; Catalog No.: 10714011; Product…

March 3, 2026 · Medical device recalls Moderate risk The affected devices contain a manufacturing defect which may prevent the appro…

Angiodynamics, Inc. recalls AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 21 R/O Markers; ACCU-VU OF 4F X 70CM 035 NB 6SH 21 R/O 1CM;…

March 3, 2026 · Medical device recalls Moderate risk The affected devices contain a manufacturing defect which may prevent the appro…

Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter, Cobra (2), Non-Braided; SOFT-VU CB2 4F X 100CM 038 NB 0SH; Catalog No.: 10714018; Produc…

March 3, 2026 · Medical device recalls Moderate risk The affected devices contain a manufacturing defect which may prevent the appro…

Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter, Sos Omni Selective (1), Non-Braided; SOFT-VU SO1 4F X 80CM 038 NB 0SH; Catalog No.: 1071…

March 3, 2026 · Medical device recalls Moderate risk The affected devices contain a manufacturing defect which may prevent the appro…

Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter, Straight Art, Non-Braided; SOFT-VU STR ART 4F X 65CM 035 NB 0SH; Catalog No.: 10731401;…

March 3, 2026 · Medical device recalls Moderate risk The affected devices contain a manufacturing defect which may prevent the appro…

Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter, Pigtail, Non-Braided; SOFT-VU PT 4F X 100CM 035 NB 10SH; Catalog No.: 10707103; Product/…

March 3, 2026 · Medical device recalls Moderate risk The affected devices contain a manufacturing defect which may prevent the appro…

Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter, Omni Flush, Non-Braided; SOFT-VU OF 4F X 65CM 035 NB 6SH; Catalog No.: 10732301; Product…

March 3, 2026 · Medical device recalls Moderate risk The affected devices contain a manufacturing defect which may prevent the appro…

Angiodynamics, Inc. recalls AccuVu Angiographic Catheter, Pigtail, Non-Braided, With 21 R/O Markers; ACCU-VU PT 4F X 70CM 035 NB 10SH 21 R/O 1CM; C…

March 3, 2026 · Medical device recalls Moderate risk The affected devices contain a manufacturing defect which may prevent the appro…

Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter, Cobra (1), Non-Braided; SOFT-VU CB1 4F X 100CM 038 NB 0SH; Catalog No.: 10714017; Produc…

March 3, 2026 · Medical device recalls Moderate risk The affected devices contain a manufacturing defect which may prevent the appro…

Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter, Berenstein, Non-Braided; SOFT-VU BER 4F X 65CM 038 NB 0SH; Catalog No.: 10714009; Produc…

March 3, 2026 · Medical device recalls Moderate risk The affected devices contain a manufacturing defect which may prevent the appro…

Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter, Omni Flush, Non-Braided; SOFT-VU OF 4F X 65CM 038 NB 6SH; Catalog No.: 10714001; Product…

March 3, 2026 · Medical device recalls Moderate risk The affected devices contain a manufacturing defect which may prevent the appro…

Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 40CM 035 NB 0SH; Catalog No.: 10734301; Product/UPN…

March 3, 2026 · Medical device recalls Moderate risk The affected devices contain a manufacturing defect which may prevent the appro…

Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter, Pigtail, Non-Braided; SOFT-VU PT 4F X 65CM 038 NB 10SH; Catalog No.: 10714002; Product/U…

March 3, 2026 · Medical device recalls Moderate risk The affected devices contain a manufacturing defect which may prevent the appro…

Angiodynamics, Inc. recalls AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 2 R/O Markers; ACCU-VU OF 4F X 70CM 035 NB 6SH 2 R/O 2CM; C…

March 3, 2026 · Medical device recalls Moderate risk The affected devices contain a manufacturing defect which may prevent the appro…

Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 100CM 038 NB 0SH; Catalog No.: 10714021; Product/UP…

March 3, 2026 · Medical device recalls Moderate risk The affected devices contain a manufacturing defect which may prevent the appro…

Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter, Berenstein, Non-Braided; SOFT-VU BER 4F X 100CM 038 NB 0SH; Catalog No.: 10714016; Produ…

March 3, 2026 · Medical device recalls Moderate risk The affected devices contain a manufacturing defect which may prevent the appro…

Angiodynamics, Inc. recalls AccuVu Angiographic Catheter, Straight Flush, Non-Braided, With 10 R/O Markers; ACCU-VU STR FL 4F X 100CM 035 NB 6SH 10…

March 3, 2026 · Medical device recalls Moderate risk The affected devices contain a manufacturing defect which may prevent the appro…

Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 65CM 038 NB 0SH; Catalog No.: 10714014; Product/UPN…

March 3, 2026 · Medical device recalls Moderate risk The affected devices contain a manufacturing defect which may prevent the appro…

Angiodynamics product recalled over labeling errors

February 4, 2025 · Medical device recalls Moderate risk Product is mislabeled with the incorrect fill volume.

Angiodynamics, Inc. recalls AURYON LASER SYSTEM 100-120 VAC. Model Number: EXM001. Product Number: EXM-2001-1100

November 25, 2024 · Medical device recalls Moderate risk Potential for procedural delays or interruptions during use of the Auryon Ather…