by The agency faulted the device maker for delayed notice of mounting complications, citing increasing reports of how use of the device perforated the walls of the heart.The agency faulted the device maker for delayed notice of mounting complications, citing increasing reports of how use of the device perforated the walls of the heart.Read MoreMedical Devices, Recalls and Bans of Products, Heart, Deaths (Fatalities), Implants, Elderly, Food and Drug Administration, impella, Abiomed Inc, Johnson & Johnson, your-feed-healthcareNYT > Health
