Medtronic MDT underwent analysis by 15 analysts in the last quarter, revealing a spectrum of viewpoints from bullish to bearish. The following table provides a quick overview of their recent ...
With this approval, Medtronic is now the first and only company with two PFA technologies available for patients with Afib. The PulseSelectâ„¢ Pulsed Field Ablation System, which was FDA approved ...
In its initial July Safety Alert, the New Jersey-based medical device company Medtronic announced ... all MiniMed 600 series ...
The U.S. Food and Drug Administration on Thursday announced a Class 1 recall for Medtronic MiniMed 600- and 700-series insulin pumps because of an increased risk of shorter battery life that could ...
WARSAW — Medtronic is notifying users of MiniMed 600 and 700 series insulin pumps of an increased risk for reduced battery life and less time until shutdown after a battery alert occurs. Pumps that ...
Affecting all lots, serial numbers, and these models of the MiniMed 630G, 670G, 770G, and 780G products ... sooner than usually expected." Medtronic said this battery issue could happen either ...
In its initial July Safety Alert, the New Jersey-based medical device company Medtronic announced that it ... series insulin pump models—and in particular, MiniMed™ 630G, MiniMed™ 670G, MiniMed™ 770G, ...
Medtronic has issued a second alert letter to patients regarding shortened battery life of the MiniMed 600 and 700 series insulin pumps. The affected products include the MiniMed 630G, 670G, 770G ...
Medtronic has issued a voluntary recall on ... The Dublin-based medical-device maker said Friday that customers of its MiniMed 600 series or 700 series insulin pumps have reported shortened ...
Pedersen's POV graphic featuring MD+DI Senior Editor Amanda Pedersen and her quote about 23andMe. Pedersen's POV is a weekly op-ed about medtech.