WASHINGTON--Patients with type 1 diabetes who use Medtronic's MiniMedTM 670G insulin pump system are able to maintain blood glucose levels in the targeted range over 71% of the time, according to a ...
DUBLIN, Sept. 09, 2019 (GLOBE NEWSWIRE) -- Medtronic plc (NYSE:MDT), the global leader in medical technology, services and solutions, today announced it has secured reimbursement for the MiniMed™ 670G ...
Medtronic plc.'s MDT Diabetes Management segment is dominating the headlines of late. Following the company’s receipt of the CE Mark approval for its advanced continuous glucose monitoring (CGM) ...
(CNN) --Medtronic has recalled some of its insulin pumps after injuries and one death were reported due to the device malfunctioning, according to a US Food and Drug Administration announcement on ...
Medtronic is recalling more than 322,000 MiniMed insulin pumps because a faulty locking mechanism may cause incorrect dosing. The flaw could prove fatal to the type 1 diabetics who rely on the devices ...
Medtronic is warning of a potential safety risk involving its MiniMed insulin pumps that has led to at least one hospitalization and one death, according to the Star Tribune. Medtronic said its ...
(CNN) -- Medtronic has recalled some of its insulin pumps after injuries and one death were reported due to the device malfunctioning, according to a US Food and Drug Administration announcement on ...
Several types of insulin pumps are being recalled by a medical device company because of a dangerous flaw that could affect more than 322,000 users with Type 1 diabetes. The Food and Drug ...
Health care technology company Medtronic recalled more than 300 thousand MiniMed 600 Series insulin pumps Wednesday in a Class I recall after thousands of injuries and one death. Medtronic recalled ...
Medtronic has recalled some of its insulin pumps after injuries and one death were reported due to the device malfunctioning, according to a US Food and Drug Administration announcement on Wednesday.
Medtronic has recalled some of its insulin pumps after injuries and one death were reported due to the device malfunctioning, according to a US Food and Drug Administration announcement on Wednesday.
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