Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF): Medical Device Recalls in 2020

According to to data from the FDA, there were 11 medical device recalls made by Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) in 2020. See the details of the recalls below.

You can see similar recalls for other firms.

• Solara CRT-P MRI, Model Numbers: a) W1TR03, b) W1TR06, c) W4TR03, d) W4TR06
• Serena CRT-P MRI, Model Numbers: a) W1TR02, b) W1TR05, c) W4TR02, d) W4TR05
• Azure XT DR MRI, Model Numbers: a) W1DR01 and b) W2DR01
• CareLink SmartSync Device Manager, Model Number 24970A
• Percepta CRT-P MRI, Model Numbers: a) W1TR01, b) W1TR04, c) W4TR01, d) W4TR04
• Azure S DR MRI, Model Number W3DR01
• Azure XT SR MRI, Model Numbers: a) W1SR01 and b) W2SR01
• Azure S SR MRI, Model Number W3SR01
• Medtronic CareLink Encore 29901 Programmer. Used to interrogate and program Medtronic and Vitatron implantable devices, such as pacemaker/ICD/CRT.
• Medtronic CareLink 2090 Programmer. Used to interrogate and program Medtronic and Vitatron implantable devices, such as pacemaker/ICD/CRT.
• Patient Connector, Model Number 24967