Haemonetics Corporation - CS Bowl Set - Class 2 Recall
JAPAN DISP SET, 261J, 205J, HAR - Product Usage: its related accessory components are intended to be used for the recovery and processing of blood shed during or subsequent to an operation or as a result of trauma. The recovered blood is processed by a centrifugation and washing procedure before pumping the red cell product to either a bag for gravity reinfusion into the patient or an extracorporeal circuit. (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 30, 2020 Category: Medical Devices Source Type: alerts
Haemonetics Corporation - CS Set - Class 2 Recall
JAPAN LOW VOL(125ML) CS5 SET,LN 261J - Product Usage: its related accessory components are intended to be used for the recovery and processing of blood shed during or subsequent to an operation or as a result of trauma. The recovered blood is processed by a centrifugation and washing procedure before pumping the red cell product to either a bag for gravity reinfusion into the patient or an extracorporeal circuit. (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 30, 2020 Category: Medical Devices Source Type: alerts
Haemonetics Corporation - CSE Set - Class 2 Recall
JAPAN CELL SAVER ELITE SET - 225ML - Product Usage: its related accessory components are intended for use to recover blood shed during or subsequent to an operation or as a result of trauma, processing the blood by a centrifugation and washing procedure, and pumping this processed red cell product to either a bag for gravity reinfusion into the patient or to the arterial line of an extracorporeal circuit for reinfusion into the patient. (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 30, 2020 Category: Medical Devices Source Type: alerts
Haemonetics Corporation - CS Bowl Set - Class 2 Recall
JAPAN DISP SET, 261J, 205J, 208 - Product Usage: its related accessory components are intended to be used for the recovery and processing of blood shed during or subsequent to an operation or as a result of trauma. The recovered blood is processed by a centrifugation and washing procedure before pumping the red cell product to either a bag for gravity reinfusion into the patient or an extracorporeal circuit. (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 30, 2020 Category: Medical Devices Source Type: alerts
Haemonetics Corporation - CSE Fastpack Set - Class 2 Recall
JAPAN CS ELITE FASTPACK, 225ML - Product Usage: its related accessory components are intended for use to recover blood shed during or subsequent to an operation or as a result of trauma, processing the blood by a centrifugation and washing procedure, and pumping this processed red cell product to either a bag for gravity reinfusion into the patient or to the arterial line of an extracorporeal circuit for reinfusion into the patient. (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 30, 2020 Category: Medical Devices Source Type: alerts
Haemonetics Corporation - CS5 Set - Class 2 Recall
Japan DISP SET, 263J, 205J, HAR - Product Usage: its related accessory components are intended to be used for the recovery and processing of blood shed during or subsequent to an operation or as a result of trauma (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 30, 2020 Category: Medical Devices Source Type: alerts
Haemonetics Corporation - CS5 Bowl Kit - Class 2 Recall
Japan DISP SET, 263J, 205J, 208 - Product Usage: its related accessory components are intended to be used for the recovery and processing of blood shed during or subsequent to an operation or as a result of trauma (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 30, 2020 Category: Medical Devices Source Type: alerts
Haemonetics Corporation - CSE Fastpack Set - Class 2 Recall
Japan CS Elite FASTPACK DISP. SET - 125ML - Product Usage: its related accessory components are intended for use to recover blood shed during or subsequent to an operation or as a result of trauma, processing the blood by a centrifugation and washing procedure, and pumping this processed red cell product to either a bag for gravity reinfusion into the patient or to the arterial line of an extracorporeal circuit for reinfusion into the patient. (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 30, 2020 Category: Medical Devices Source Type: alerts
Haemonetics Corporation - CSE Set - Class 2 Recall
JAPAN CELL SAVER ELITE SET - 125ML - Product Usage: its related accessory components are intended for use to recover blood shed during or subsequent to an operation or as a result of trauma, processing the blood by a centrifugation and washing procedure, and pumping this processed red cell product to either a bag for gravity reinfusion into the patient or to the arterial line of an extracorporeal circuit for reinfusion into the patient. (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 30, 2020 Category: Medical Devices Source Type: alerts
Medtronic Navigation, Inc. - Medtronic Percutaneous Pin Adapter - Class 2 Recall
Medtronic Adapter Percutaneous Pin, REF 9734752 (GTIN 00643169529489) and REF 9734752-G02 (GTIN 00763000054915), contained in the following kits: Upgrade Set Percutaneous Pin, REF 9735502 (GTIN 00643169529533) and REF 9735502-G02 (GTIN 00763000208462); Medtronic Adapter Percutaneous Pin Kit, REF 9734752K (GTIN 00643169540521); and Medtronic Adapter Percutaneous Pin Kit, REF 9734752K (GTIN 00643169641006) (Japan). The percutaneous pin adapter is a component of the StealthAir Frame Assembly. (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 20, 2019 Category: Medical Devices Source Type: alerts
Terumo Cardiovascular Systems Corporation - Terumo Capiox NX19 Oxygenator - Class 2 Recall
Terumo Capiox NX19 Oxygenator (East Orientation), P/N: CXOT280 Exported only to Japan for inclusion into convenience kits that are sold only within the Japanese market (Source: Medical Device Recalls)
Source: Medical Device Recalls - July 31, 2019 Category: Medical Devices Source Type: alerts
Terumo Cardiovascular Systems Corporation - Capiox NX19 Oxygenator - Class 2 Recall
Terumo Capiox NX19 Oxygenator (West Orientation P/N:CXOT281 Exported only to Japan for inclusion into convenience kits that are sold only within the Japanese market (Source: Medical Device Recalls)
Source: Medical Device Recalls - July 31, 2019 Category: Medical Devices Source Type: alerts
ANTI-BACTERIAL HAND JAPANESE CHERRY BLOSSOM (Alcohol) Gel [Bath Body Works, Inc.]
Updated Date: Jul 1, 2019 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - July 1, 2019 Category: Drugs & Pharmacology Source Type: alerts
Accuray Incorporated - CyberKnife M6 - Class 2 Recall
CyberKnife VSI, Part Numbers: a) 032500-010: CyberKnife VSI 9.6.x Robotic Radiosurgery System for Japan b) 033000-010: CyberKnife VSI Robotic Radiosurgery System (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 2, 2019 Category: Medical Devices Source Type: alerts
Maribel ’s Sweets Inc. Allergy Alert on Undeclared Milk Allergens in Chocolate Bars
Maribel ’s Sweets Inc. of Brooklyn, NY is recalling its 2.82oz MarieBelle Japanese Matcha Japanese Green Tea and White Chocolate Bar, container code 101619, Cacao Market by MarieBelle Rosemary Truffle Salt 60% Dark Chocolate Bar, all container codes, and the Cacao Market by MarieBelle Orange Peels 60 (Source: FDA Food Alergies)
Source: FDA Food Alergies - May 16, 2019 Category: Food Science Authors: FDA Source Type: alerts
