Angiodynamics, Inc. recalls
20 recalls.
- AccuVu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - AccuVu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - AccuVu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - AccuVu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft -Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the...