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 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.
The FDA announced that Medtronic expanded two recalls relating to the MiniMed 600 series of insulin pumps and MiniMed 508 remote controllers. Both were designated by the agency as Class I, the most ...
Medtronic MiniMed insulin pumps are being recalled due to an issue that can lead to incorrect dosing. The affected pumps include the MiniMed 630G and MiniMed 670G. The recall affects 322,055 devices.
SPRINGFIELD, Mo. — The Food and Drug Administration (FDA) has issued a class I recall on certain types of Medtronic insulin pumps. A class I recall means the devices could cause serious injuries or ...
(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 ...
The FDA issued a warning to patients who use a particular insulin pump system that unauthorized people could access it and change how much insulin a patient receives. In the warning posted Sept. 20, ...
A shorter-than-expected battery life prompted a voluntary recall of certain insulin pumps from Medtronic's MiniMed 600 and 700 series, the FDA detailed on Thursday. Affecting all lots, serial numbers, ...
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 ...
Medical device major Medtronic plc’s MDT MiniMed 630G system with SmartGuard technology – a new insulin pump that facilitates diabetes care – recently won the U.S. FDA (Food and Drug Administration) ...
(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 ...
Results that may be inaccessible to you are currently showing.
Hide inaccessible results