Sponsored By
Medtronic Devices Recalled Over 'Manufacturing Error'
Materials
Medtronic Devices Recalled Over 'Manufacturing Error'Medtronic Devices Recalled Over 'Manufacturing Error'
FDA has issued a Class I recall for some Medtronic ICDs and CRT-Ds impacted by a manufacturing defect that could prevent them from delivering the shock needed to pace a patient's heart or revive a patient in cardiac arrest.
Sign up for the QMED & MD+DI Daily newsletter.