Impella Devices Recalled After Deaths, Injuries Tied to TAVR Interactions
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 8,000 blood pumps marketed as Impella 5.0, Impella CP, Impella 2.5, Impella CP with SmartAssist, Impella LD, or Impella…
bubmagJuly 28, 2023