Medtronic Recalls HeartWare HVAD System Batteries for Electrical Faults That Cause Battery Failure
An electrical fault may cause the batteries of the HeartWare HVAD System to fail, leading to severe injury or death.
An electrical fault may cause the batteries of the HeartWare HVAD System to fail, leading to severe injury or death.
Wed, 24 Aug 2022 14:47:42 -0400
Dans le traitement de la cardiomyopathie hypertrophique obstructive symptomatique chez l'adulte.
Mon, 22 Aug 2022 15:15:59 -0400
Hospira, Inc., a Pfizer company, is voluntarily recalling one lot of Propofol Injectable Emulsion (containing benzyl alcohol), 100mL Single Patient Use Glass Fliptop Vial; lot EA7470, to the user level due to visible particulates observed in two vials during annual examination of retention samples.
Fri, 19 Aug 2022 11:39:54 -0400
Fri, 19 Aug 2022 11:37:10 -0400
Fri, 19 Aug 2022 11:30:47 -0400
Fri, 19 Aug 2022 11:28:48 -0400
Fri, 19 Aug 2022 11:15:14 -0400
Fri, 19 Aug 2022 10:43:13 -0400
80.211.154.110