valitude crt-pvalitude crt-p (u125-u128); visionist crt-p models u225, u226, and u228; resonate crt-d models g424, g425, g426, g428, g437, g447, g448, g524, g525, g526, g528, g537, g547, g548; vigilant crt-d models g224, g225, g228, g237, g247, g248; momentum crt-d models g124, g125, g126, g128, g138; charisma crt-d models g324, g325, g328, g337, g347, g348; autogen crt-d models g160, g161, g166, g168 (us models), g172, g173, g175, g177, g179; dynagen crt-d models g150, g151, g156, g158; inogen crt-d models g140, g141, g146, g148; origen crt-d models g050, g051, g056, g058

“We take a patient-first approach to assessing the applicability of every recall and communicate to regulatory bodies in all geographies where the recalled device is sold,” Boston Scientific said in a statement to ICIJ. “We have coordinated several recalls across many countries in a timely manner,” the company said, adding that it complies with all national laws, which can often vary and require different processes for reporting information or taking action on recalls. The company said it uses a rigorous and uniform process to take action on recalls and that “when we initiate a field action (e.g. recall, safety alert), every customer who has received an affected product receives a communication that includes a letter for the physician.”