FLU EASE (cairina moschata heart/liver autolysate) pellet [WFM Private Label, LP]
Updated Date: Thu, 05 Oct 2023 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - October 5, 2023 Category: Drugs & Pharmacology Source Type: alerts
Baxter Healthcare Corporation - Baxter Epiphany - Class 2 Recall
Baxter Epiphany Cardio Server E3 ECG Management System Servers with software versions: a) v6.1.x, b) v6.2.x, c) v7.0.x. (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 29, 2023 Category: Medical Devices Source Type: alerts
MYOCARD SARCODE (leonurus cardiaca, valeriana officinalis, cactus grandiflorus, convallaria majalis, spigelia anthelmia, heart (bovine), veratrum album, arteria suis, aurum muriaticum natronatum, digitalis purpurea, kali carbonicum) spray [Nutritional Specialties, Inc.]
Updated Date: Thu, 28 Sep 2023 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - September 28, 2023 Category: Drugs & Pharmacology Source Type: alerts
CARDIOVASCULAR FORMULA (cactus grandiflorus, spigelia anthelmia, kalmia latifolia, arsenicum album, strophanthus hispidus, scilla maritima, digitalis purpurea, phosphorus, kali carbonicum) spray [Nutritional Specialties, Inc.]
Updated Date: Mon, 25 Sep 2023 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - September 25, 2023 Category: Drugs & Pharmacology Source Type: alerts
GE Medical Systems Information Technologies Inc - Prucka 3 Amplifiers, Field Replaceable Units - Class 2 Recall
Prucka 3 Amplifiers, Model P1801PA, and Field Replaceable Units (FRUs), Model 5875569, used with CardioLab AltiX and ComboLab AltiX. (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 20, 2023 Category: Medical Devices Source Type: alerts
Abbott Medical - Gallant/Neutrino/Entrant CRTD - Class 2 Recall
Gallant HF Cardiac Resynchronization Therapy Defibrillator: HF CRT-D REF CDHFA500Q Neutrino HF Cardiac Resynchronization Therapy Defibrillator: NxT HF CRT-D REF CDHFA600Q Entrant HF Cardiac Resynchronization Therapy Defibrillator : HF CRT-D REF CDHFA300Q The primary function of ICDs and CRT-Ds are to treat life-threatening ventricular tachyarrhythmias via anti-tachycardia pacing (ATP), or cardioversion/defibrillation. Implantable Cardioverter Defibrillators (ICDs) can either be a dual chamber (also known as DR if rate responsive) device that is connected to a right atrial (RA) pacing lead and right ventricular defibrill...
Source: Medical Device Recalls - September 20, 2023 Category: Medical Devices Source Type: alerts
Abbott Medical - Gallant/Neutrino/Entrant ICD - Class 2 Recall
Gallant VR Implantable Cardioverter Defibrillator: VR ICD REF CDVRA500Q Gallant DR Implantable Cardioverter Defibrillator: DR ICD REF CDDRA500Q Neutrino VR Implantable Cardioverter Defibrillator: NxT VR ICD REF CDVRA600Q Neutrino DR Implantable Cardioverter Defibrillator: NxT DR ICD REF CDDRA600Q Entrant VR Implantable Cardioverter Defibrillator: VR ICD REF CDVRA300Q Entrant DR Implantable Cardioverter Defibrillator: DR ICD REF CDDRA300Q The primary function of ICDs and CRT-Ds are to treat life-threatening ventricular tachyarrhythmias via anti-tachycardia pacing (ATP), or cardioversion/defibrillation. Implantable Cardio...
Source: Medical Device Recalls - September 20, 2023 Category: Medical Devices Source Type: alerts
Datascope Corp. - Cardiosave Hybrid - Class 2 Recall
Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-31, 0998-UC-0800-31, 0998-00-0800-32, 0998-00-0800-33, 0998-UC-0800-33, 0998-00-0800-34, 0998-00-0800-35, 0998-00-0800-45, 0998-00-0800-52, 0998-UC-0800-52, 0998-00-0800-53, 0998-UC-0800-53, 0998-00-0800-55, 0998-UC-0800-55, 0998-00-0800-65 (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 1, 2023 Category: Medical Devices Source Type: alerts
Datascope Corp. - Cardiosave Rescue - Class 2 Recall
Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85 (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 1, 2023 Category: Medical Devices Source Type: alerts
Datascope Corp. - Cardiosave Rescue - Class 1 Recall
Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85 (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 31, 2023 Category: Medical Devices Source Type: alerts
Datascope Corp. - Cardiosave Hybrid - Class 1 Recall
Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-31, 0998-UC-0800-31, 0998-00-0800-32, 0998-00-0800-33, 0998-UC-0800-33, 0998-00-0800-34, 0998-00-0800-35, 0998-00-0800-45, 0998-00-0800-52, 0998-UC-0800-52, 0998-00-0800-53, 0998-UC-0800-53, 0998-00-0800-55, 0998-UC-0800-55, 0998-00-0800-65 (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 31, 2023 Category: Medical Devices Source Type: alerts
Datascope Corp. - Cardiosave Rescue - Class 1 Recall
Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85 (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 31, 2023 Category: Medical Devices Source Type: alerts
Datascope Corp. - Cardiosave Hybrid - Class 1 Recall
Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-31, 0998-UC-0800-31, 0998-00-0800-32, 0998-00-0800-33, 0998-UC-0800-33, 0998-00-0800-34, 0998-00-0800-35, 0998-00-0800-45, 0998-00-0800-52, 0998-UC-0800-52, 0998-00-0800-53, 0998-UC-0800-53, 0998-00-0800-55, 0998-UC-0800-55, 0998-00-0800-65 (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 31, 2023 Category: Medical Devices Source Type: alerts
Datascope Corp. - Cardiosave Rescue - Class 1 Recall
Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85 (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 31, 2023 Category: Medical Devices Source Type: alerts
