Company page

Angiodynamics, Inc. alerts

Verified recalls, refunds, lawsuits, and settlements involving Angiodynamics, Inc..

Recall Active FDA Official source

Angiodynamics, Inc.: Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 65CM 038 NB 0SH;...

The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. Product details:...

Company: Angiodynamics, Inc.
Deadline: No deadline listed
Source: U.S. Food and Drug Administration

View affected products Official source

Recall Active FDA Official source

Angiodynamics, Inc.: AccuVu Angiographic Catheter, Straight Flush, Non-Braided, With 10 R/O Markers; ACCU-VU...

The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. Product details:...

Company: Angiodynamics, Inc.
Deadline: No deadline listed
Source: U.S. Food and Drug Administration

View affected products Official source

Recall Active FDA Official source

Angiodynamics, Inc.: Soft-Vu Angiographic Catheter, Berenstein, Non-Braided; SOFT-VU BER 4F X 100CM 038 NB...

The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. Product details:...

Company: Angiodynamics, Inc.
Deadline: No deadline listed
Source: U.S. Food and Drug Administration

View affected products Official source