Medtronic Vascular FDA Recalls

5 recalls on file across devices, 1 of them Class I and 0 still open. Matched by name to MDT.

Newest first

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

Product	Reason	Class	Initiated
Angiographic Guidewire Component: Model Number: 107042, 107044, 107447, 110003, 110004, The angiographic guidewire cClass IMay 4, 2021The component part numbers intended for shipment to a third-	The component part numbers intended for shipment to a third-party, where they are further processed into kits	Class IDevices	May 4, 2021
Medtronic 6F Launcher Guide Catheter 100 cm EBU 3.0 Model Number: LA6EBU30Class IIJan 15, 2021Sterility may be compromised due to an unsealed pouch	Sterility may be compromised due to an unsealed pouch	Class IIDevices	Jan 15, 2021
Medtronic 6F Launcher Guide Catheter 100 cmJL 3.5 Model Number: LA6JL35Class IIJan 15, 2021Sterility may be compromised due to an unsealed pouch	Sterility may be compromised due to an unsealed pouch	Class IIDevices	Jan 15, 2021
Medtronic 6F Launcher Guide Catheter 100cm EBU 3.75 Model Number: LA6EBU375Class IIJan 15, 2021Sterility may be compromised due to an unsealed pouch	Sterility may be compromised due to an unsealed pouch	Class IIDevices	Jan 15, 2021
Medtronic 6F Launcher Guide Catheter 100 cm JR 4.0 Model Number: LA6JR40Class IIJan 15, 2021Sterility may be compromised due to an unsealed pouch	Sterility may be compromised due to an unsealed pouch	Class IIDevices	Jan 15, 2021