FEMALE STIMULANT (lilium tigrinum, bovista, cypripedium pubescens, hydrastis canadensis, petroselinum sativum, aquilegia vulgaris, funiculus umbilicalis suis, glandula suprarenalis suis, heart (suis), kreosotum, oophorinum (suis), uterus (suis), folliculinum, lachesis mutus, magnesia phosphorica, mercurius solubilis, sepia, pineal gland (suis), hypophysis suis, aconiticum acidum cis-, apis venenum purum, estradiol, progesterone, testosterone, placenta totalis suis, faecalis (alkaligenes), mutabile bacillus (bach)) liquid [Deseret Biologicals, Inc.]
Updated Date: Tue, 20 Feb 2024 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - February 20, 2024 Category: Drugs & Pharmacology Source Type: alerts
HEART LIQUESCENCE (ginkgo biloba, leonurus cardiaca, cactus grandiflorus, heart (bovine), taurine, strophanthus hispidus, ubidecarenonum (coq10), aurum muriaticum natronatum, magnesia phosphorica) liquid [Nutritional Specialties, Inc.]
Updated Date: Mon, 19 Feb 2024 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - February 19, 2024 Category: Drugs & Pharmacology Source Type: alerts
HEART LIQUESCENCE (ginkgo biloba, leonurus cardiaca, cactus grandiflorus (n), heart (bovine), taurine, ubidecarenonum (coq 10), aurum muriaticum natronatum, magnesia phosphorica) liquid [Nutritional Specialties, Inc.]
Updated Date: Mon, 19 Feb 2024 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - February 19, 2024 Category: Drugs & Pharmacology Source Type: alerts
Maquet Medical Systems USA - HLS Set Advanced 5.0 - Class 2 Recall
Model No. BEQ-HLS 5050 USA, HLS Set Advanced 5.0, Product Code/Part Number 70106.9077. Used with the CARDIOHELP heart-lung machine. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 14, 2024 Category: Medical Devices Source Type: alerts
Maquet Medical Systems USA - HLS Set Advanced 7.0 - Class 2 Recall
BEQ-HLS 7050 USA, HLS Set Advanced 7.0, Product Code/Part Number 70106.9078. Used with the CARDIOHELP heart-lung machine. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 14, 2024 Category: Medical Devices Source Type: alerts
OSCILLOCOCCINUM (cairina moschata heart/liver autolysate) pellet [Laboratoires Boiron]
Updated Date: Fri, 09 Feb 2024 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - February 9, 2024 Category: Drugs & Pharmacology Source Type: alerts
Maquet Medical Systems USA - ROTAFLOW - Class 2 Recall
BO-RF-32-USA RotaFlow Centrifugal Pump with SOFTLINE Coating, Product Code 701047553. For use with an extracorporeal cardiovascular or cardiopulmonary bypass circuit. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 3, 2024 Category: Medical Devices Source Type: alerts
Maquet Medical Systems USA - ROTAFLOW - Class 2 Recall
BEQ-RF-32-USA RotaFlow Centrifugal Pump with BIOLINE Coating, Product Code 701047554. For use with an extracorporeal cardiovascular or cardiopulmonary bypass circuit. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 3, 2024 Category: Medical Devices Source Type: alerts
American Contract Systems, Inc. - Custom procedural convenience kits and trays - Class 2 Recall
Procedural convenience kits and trays, cardiac, labeled as: a) EP LAB BI V IMPLANT PACK, kit number AGBI64J; b) LAB DEVICE IMPLANT, kit number AGDI40J; c) LAB DEVICE IMPLANT, kit number AGDI40K; d) MINOR VASCULAR, kit number AGMV26O; e) OPEN HEART ACCESSORY, kit number AGOH98Q; f) OPEN HEART ACCESSORY, kit number AGOH98R; g) OPEN HEART ACCESSORY, kit number AGOH98S; h) PERIPHERAL VASCULAR, kit number AGPV28O; i) PERIPHERAL VASCULAR, kit number AGPV28P; j) MINOR VASCULAR, kit number AHMV26J; k) MINOR VASCULAR, kit number AHMV26K; l) HEART PACK - 205947, kit number ANCV78AX; m) HEART PACK - 205947 , kit number A...
Source: Medical Device Recalls - January 27, 2024 Category: Medical Devices Source Type: alerts
American Contract Systems, Inc. - Custom procedural convenience kits and trays - Class 2 Recall
Custom procedural convenience kits and trays, anesthesia, labeled as: a) HEART ANESTHESIA BUNDLE NS, Kit Number LMHA01V; b) OR/Anesthesia Central Line Insertion Kit, Kit Number UIAN43L (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 27, 2024 Category: Medical Devices Source Type: alerts
American Contract Systems, Inc. - Custom procedural convenience kits and trays - Class 2 Recall
Custom procedural convenience kits and trays, cardiac, labeled as: a) HEART CATHETERIZATION TRAY, kit number JRHC45G; b) TAVR PACK, kit number LLTV10; c) CATH PED LF SJH, kit number SJCA21F; d) CATH HEART ADL LF SJH, kit number SJCH22F; e) INT RAD PORTS-LF - 206060, kit number UDIR58AL (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 27, 2024 Category: Medical Devices Source Type: alerts
VASCU-PRO T009 (cactus grandiflorus, hamamelis virginiana, valeriana officinalis, arteria suis, heart (suis), arnica montana, aurum metallicum, baryta muriatica, cholesterinum, lecithin, magnesia muriatica, oxalicum acidum, phosphorus) liquid [Guangzhou Renuma Medical Systems Co., Ltd]
Updated Date: Wed, 24 Jan 2024 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - January 24, 2024 Category: Drugs & Pharmacology Source Type: alerts
Medtronic Inc. - Medtronic Cobalt - Class 2 Recall
Cobalt XT DR MRI SureScan Implantable Cardioverter Defibrillator, product number DDPA2D1 (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 23, 2024 Category: Medical Devices Source Type: alerts
Maquet Cardiovascular, LLC - Atrium Express Dry Suction Dry Seal Chest Drain - Class 1 Recall
Product REF 4050-100N, DRAIN, EXPRESS BRU W/AC, Blood Recovery Unit (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 13, 2024 Category: Medical Devices Source Type: alerts
Maquet Cardiovascular, LLC - Atrium Express Dry Suction Dry Seal Chest Drain - Class 1 Recall
Product REF 4000-100N, DRAIN, EXPRESS SINGLE W/AC, Single Collection (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 13, 2024 Category: Medical Devices Source Type: alerts
