Angiodynamics Inc. (Navilyst Medical Inc.) FDA Recalls

2 recalls on file across devices, 0 of them Class I and 0 still open. Matched by name to ANGO.

Newest first

Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product	Reason	Class	Initiated
Smart Port CT-Implantable Port Catalogue #: CT96STSD-VI, CT96STSA-VI - Product Usage: indicated for any patient requirinClass IIFeb 22, 2021AngioDynamics, Inc. is recalling a specific batch of AngioDy	AngioDynamics, Inc. is recalling a specific batch of AngioDynamics Implantable Infusion Port kits and Valved i	Class IIDevices	Feb 22, 2021
AngioDynamics Safe Sheath Ultralite - Vascular Introducer/Catheter Introducer Catalogue #: VI10 - Product Usage: For tClass IIFeb 22, 2021AngioDynamics, Inc. is recalling a specific batch of AngioDy	AngioDynamics, Inc. is recalling a specific batch of AngioDynamics Implantable Infusion Port kits and Valved i	Class IIDevices	Feb 22, 2021