Impella Devices Recalled After Deaths, Injuries Tied to TAVR Interactions

(MedPage Today) -- More Impella left-sided blood pumps are under Class I recall, this time for potential interactions with transcatheter aortic valve replacement (TAVR) stents, the FDA announced Thursday.
The affected devices include nearly 8...

Source: MedPage Today Public Health - July 28, 2023 Category: American Health Source Type: news