PLUS RINSE EMERGENCY EYEWASH (Purified Water) Liquid [INNOVATIVE SAFETY SUPPLY INC.]
Updated Date: May 7, 2019 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - May 7, 2019 Category: Drugs & Pharmacology Source Type: alerts
ALOCANE EMERGENCY BURN (Lidocaine Hydrochloride) Gel [Quest Products, LLC.]
Updated Date: May 1, 2019 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - May 1, 2019 Category: Drugs & Pharmacology Source Type: alerts
Maquet Cardiovascular Us Sales, Llc - Cardiohelp Emergency Drive - Class 1 Recall
Cardiohelp Emergency Drive, Part No. 70104.8002 Product Usage: The Cardiohelp Emergency Drive is used in emergencies to manually drive the disposable if the Cardiohelp-i fails. (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 29, 2019 Category: Medical Devices Source Type: alerts
Shimadzu Medical Systems Usa Com - MobileDaRt Evolution, Mobile XRay System - Class 2 Recall
SHIMADZU MobileDaRt Evolution (MX8 Version), Mobile X-Ray System Product Usage: This device is intended to be used to take a film, CR or general radiography of patients in the hospital who cannot move and/or of outpatients in emergency. Exposure can be captured on film, CR or Digital Radiography (DR). (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 22, 2019 Category: Medical Devices Source Type: alerts
Fujifilm Medical Systems U.S.A., Inc. - Fujifilm FDR Go PLUS - Class 2 Recall
Fujifilm FDR Go PLUS, Mobile X-Ray System Product Usage: This device is intended to be used to take a film, CR or general radiography of patients in the hospital who cannot move and/or of outpatients in emergency. Exposure can be captured on film, CR or Digital Radiography (DR)> (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 22, 2019 Category: Medical Devices Source Type: alerts
Cook Medical Incorporated - Gunther Tulip Vena Cava Filter Set - Class 3 Recall
Gunther Tulip Vena Cava Filter Set for Femoral and Jugular Vein Approach, Catalog Number IGTCFS-65-1-UNl-TULIP Product Usage: The Gunther Tulip Filter is intended for the prevention of recurrent pulmonary embolism (PE) via placement in the vena cava in the following situations:(1) Pulmonary thromboembolism when anticoagulant therapy is contraindicated; (2) Failure of anticoagulant therapy in thromboembolic diseases; (3) Emergency treatment following massive PE where anticipated benefits of conventional therapy are reduced; and (4) Chronic, recurrent PE where anticoagulant therapy has failed or is contraindicated. The Filt...
Source: Medical Device Recalls - March 20, 2019 Category: Medical Devices Source Type: alerts
Cook Medical Incorporated - Cook Celect Platinum Vena Cava Filter Set - Class 3 Recall
Cook Celect Platinum Vena Cava Filter Set for Femoral and Jugular Vein Approach, Catalog Number IGTCFS-65-1-UNl-C ELECT-PT Product Usage: The Cook Celect Platinum Filter implant is intended for the prevention of recurrent pulmonary embolism (PE) via placement in the vena cava in the following situations: Pulmonary thromboembolism when anticoagulant therapy is contraindicated; Failure of anticoagulant therapy in thromboembolic diseases; Emergency treatment following massive PE where anticipated benefits of conventional therapy are reduced; and Chronic, recurrent PE where anticoagulant therapy has failed or is contraindicat...
Source: Medical Device Recalls - March 20, 2019 Category: Medical Devices Source Type: alerts
Cook Medical Incorporated - Gunther Tulip Vena Cava Filter Set - Class 3 Recall
Gunther Tulip Vena Cava Filter Set for Jugular Vein Approach, Catalog Number IGTCFS-65-1-JUG-TULIP Product Usage: The Gunther Tulip Filter implant is intended for the prevention of recurrent pulmonary embolism (PE) via placement in the vena cava in the following situations: (1) Pulmonary thromboembolism when anticoagulant therapy is contraindicated; (2) Failure of anticoagulant therapy in thromboembolic diseases; (3) Emergency treatment following massive PE where anticipated benefits of conventional therapy are reduced; and (4) Chronic, recurrent PE where anticoagulant therapy has failed or is contraindicated. The Filter ...
Source: Medical Device Recalls - March 20, 2019 Category: Medical Devices Source Type: alerts
Cook Medical Incorporated - Cook Celect Platinum Vena Cava Filter Set - Class 3 Recall
Cook Celect Platinum Vena Cava Filter Set for Femoral Vein Approach, Catalog Number IGTCFS-65-1-FEM-CELECT-PT Product Usage: The Cook Celect Platinum Filter implant is intended for the prevention of recurrent pulmonary embolism (PE) via placement in the vena cava in the following situations: Pulmonary thromboembolism when anticoagulant therapy is contraindicated; Failure of anticoagulant therapy in thromboembolic diseases; Emergency treatment following massive PE where anticipated benefits of conventional therapy are reduced; and Chronic, recurrent PE where anticoagulant therapy has failed or is contraindicated. The Filte...
Source: Medical Device Recalls - March 20, 2019 Category: Medical Devices Source Type: alerts
Cook Medical Incorporated - Cook Celect Platinum Vena Cava Filter Set - Class 3 Recall
Cook Celect Platinum Vena Cava Filter Set for Jugular Vein Approach, Catalog Number GTCFS-65-1-JUG-CELECT-PT Product Usage: The Cook Celect Platinum Filter implant is intended for the prevention of recurrent pulmonary embolism (PE) via placement in the vena cava in the following situations: Pulmonary thromboembolism when anticoagulant therapy is contraindicated; Failure of anticoagulant therapy in thromboembolic diseases; Emergency treatment following massive PE where anticipated benefits of conventional therapy are reduced; and Chronic, recurrent PE where anticoagulant therapy has failed or is contraindicated. The Filter...
Source: Medical Device Recalls - March 20, 2019 Category: Medical Devices Source Type: alerts
Cook Medical Incorporated - Gunther Tulip Vena Cava Filter Sets - Class 3 Recall
Gunther Tulip Vena Cava Filter Set for Femoral Vein Approach, Catalog Number IGTCFS-65-1-FEM-TU LIP Product Usage: The Gunther Tulip Filter implant is intended for the prevention of recurrent pulmonary embolism (PE) via placement in the vena cava in the following situations: (1) Pulmonary thromboembolism when anticoagulant therapy is contraindicated;(2) Failure of anticoagulant therapy in thromboembolic diseases; (3) Emergency treatment following massive PE where anticipated benefits of conventional therapy are reduced; and (4) Chronic, recurrent PE where anticoagulant therapy has failed or is contraindicated. The Filter ...
Source: Medical Device Recalls - March 20, 2019 Category: Medical Devices Source Type: alerts
Physio-Control Inc - LIFEPAK 15 Monitor/Defibrillator - Class 1 Recall
LIFEPAK 15 Monitor/Defibrillator Product Usage: The LIFEPAK(R) 15 Monitor/defibrillator (LP15) is a complete acute cardiac care response system designed for basic life support (BLS) and advanced life support (ALS) patient management protocols. The LP15 monitor/defibrillator is intended for use by trained medical personnel in out-of-doors and indoor emergency care settings within the environmental conditions specified in the Operating Instructions. The LP15 monitor/defibrillator is designed to be used during ground transportation except when specified otherwise. Manual mode monitoring and therapy functions are intended for...
Source: Medical Device Recalls - February 27, 2019 Category: Medical Devices Source Type: alerts
Physio-Control Inc - LIFEPAK 15 Monitor/Defibrillator - Class 1 Recall
LIFEPAK 15 Monitor/Defibrillator service kits Product Usage: The LIFEPAK(R) 15 Monitor/defibrillator (LP15) is a complete acute cardiac care response system designed for basic life support (BLS) and advanced life support (ALS) patient management protocols. The LP15 monitor/defibrillator is intended for use by trained medical personnel in out-of-doors and indoor emergency care settings within the environmental conditions specified in the Operating Instructions. The LP15 monitor/defibrillator is designed to be used during ground transportation except when specified otherwise. Manual mode monitoring and therapy functions are...
Source: Medical Device Recalls - February 27, 2019 Category: Medical Devices Source Type: alerts
EYESALINE EMERGENCY EYEWASH (Purified Water) Liquid [Honeywell Safety Products USA, Inc.]
Updated Date: Dec 24, 2018 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - December 24, 2018 Category: Drugs & Pharmacology Source Type: alerts
Philips Medical Systems Gmbh, DMC - Philips DigitalDiagnost 4.1 Chest / Emergency - Class 2 Recall
DigitalDiagnost 4.1 Chest / Emergency (Stitching Patient Support) 712029 (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 18, 2018 Category: Medical Devices Source Type: alerts
