Recalls of medical devices, diagnostic equipment, implants, and surgical instruments.
Showing 801–820 of 39,430 recalls
Angiodynamics, Inc.
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.
Angiodynamics, Inc.
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.