News & Current Events

General Medical Device Industry Research, Articles, and Information

February 12, 2020
Medtronic and the FDA were both aware of battery and wire connection defects in a now-recalled heart failure pacemaker for over a year before patients developed serious side effects, according to a report published in JAMA Internal Medicine.
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February 13, 2020:
Medtronic’s MiniMed 600 Series Insulin Pumps issued a Class I recall. 
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