B & I Overseas Trading Recalls Product Due to Potential Contamination with Listeria Monocytogenes
B&I Overseas Trading Inc from Van Nuys, CA is recalling frozen “Veladis herring in oil with Italian spices” because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, a (Source: FDA Food Safety)
Source: FDA Food Safety - December 23, 2020 Category: Food Science Authors: FDA Source Type: alerts
AROMA GURU ANTIBACTERIAL ITALIAN CITRUS (hand soap) liquid [GURUNANDA LLC]
Updated Date: Fri, 04 Dec 2020 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - December 4, 2020 Category: Drugs & Pharmacology Source Type: alerts
Arrow International Inc - AutoCAT IABP Series - Class 1 Recall
Arrow AutoCAT2 Intra-Aortic Balloon Pump AUTOCAT2 WAVE ITALIAN, Product Code IAP-0500I (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 27, 2020 Category: Medical Devices Source Type: alerts
Philips Respironics, Inc. - Trilogy EVO - Class 1 Recall
Trilogy EVO Ventilator, 02 - Italy - Model Number: IT2100X21B Trilogy Evo is intended for pediatric through adult patients weighing at least 2.5 kg. The ventilator can measure, display, record, and alarm SpO2, FiO2, CO2, and Pulse Rate data when integrated with the appropriate accessories. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 16, 2020 Category: Medical Devices Source Type: alerts
Allergy Alert Issued due to Undeclared Egg in Whole Foods Market Brand Raspberry Cheesecake Italian Gelato
Whole Foods Market is voluntarily recalling one lot code of Whole Foods Market Raspberry Cheesecake Italian Gelato because these product units contain egg that is not listed on the product label. People who have an allergy or severe sensitivity to egg run the risk of serious or life-threatening alle (Source: FDA Food Safety)
Source: FDA Food Safety - November 23, 2019 Category: Food Science Authors: FDA Source Type: alerts
VELVETGRASS (Holcus Lanatus) Solution REED CANARYGRASS (Phalaris Arundinacea) Solution BAHIA GRASS (Paspalum Notatum) Solution SMOOTH BROME (Bromus Inermis) Solution JOHNSON GRASS (Sorghum Halepense) Solution GIANT WILD RYEGRASS (Leymus Condensatus) Solution ITALIAN RYEGRASS (Lolium Multiflorum) Solution WESTERN WHEATGRASS (Pascopyrum Smithii) Solution COUCH QUACK GRASS (Elymus Repens) Solution [Greer Laboratories, Inc.]
Updated Date: Wed, 16 Oct 2019 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - October 16, 2019 Category: Drugs & Pharmacology Source Type: alerts
Italian Gluten Free Food Cl Issues Allergy Alert On Undeclared Egg In “Chef Luca’s Lasagna Al Forno – Baked Cheese Lasagna”
Italian Gluten Free Food CL of 1899 Bushwick Avenue, Merrick, NY 11566, is recalling its 15 ounce packages of “Chef Luca’s LASAGNA AL FORNO BAKED CHEESE LASAGNA” food because they may contain undeclared egg. People who have allergies to eggs run the risk of serious or life- threatening allergic reaction if they consume these products. (Source: FDA Food Alergies)
Source: FDA Food Alergies - June 5, 2019 Category: Food Science Authors: FDA Source Type: alerts
Hearthside Food Solutions Issues Allergy Alert on Undeclared Egg Allergen
Hearthside Food Solutions of Woodridge, IL is voluntarily recalling 7-Eleven ‘The Italian Job’ sandwiches, which have an incorrect information panel label that does not declare eggs as an allergen. Persons who have an allergy or severe sensitivity to eggs run the risk of serious or life-threatening (Source: FDA Food Alergies)
Source: FDA Food Alergies - May 22, 2019 Category: Food Science Authors: FDA Source Type: alerts
ICCO Cheese Company, Inc., Issues Allergy Alert on Undeclared Walnuts and Pecans in Gia Russa Whole Grain Bread Crumbs
ICCO Cheese Company is recalling Gia Russa Unseasoned Whole Grain Bread Crumbs and Gia Russa Italian Seasoned Whole Grain Bread Crumbs with “best by” dates of 08/21/2019, 09/21/2019, 10/04/2019, 11/09/2019, 11/12/2019, 12/05/2019 because they may contain undeclared walnuts and pecans. (Source: FDA Food Alergies)
Source: FDA Food Alergies - May 16, 2019 Category: Food Science Authors: FDA Source Type: alerts
VELVETGRASS (Holcus Lanatus) Solution REED CANARYGRASS (Phalaris Arundinacea) Solution BAHIA GRASS (Paspalum Notatum) Solution SMOOTH BROME (Bromus Inermis) Solution JOHNSON GRASS (Sorghum Halepense) Solution GIANT WILD RYEGRASS (Leymus Condensatus) Solution ITALIAN RYEGRASS (Lolium Multiflorum) Solution WESTERN WHEATGRASS (Pascopyrum Smithii) Solution COUCH QUACK GRASS (Elymus Repens) Solution [Greer Laboratories, Inc.]
Updated Date: Nov 14, 2018 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - November 14, 2018 Category: Drugs & Pharmacology Source Type: alerts
GE Healthcare, LLC - Aisys Anesthesia System - Class 2 Recall
Touchscreen display kit. Sold under the following product names: TOUCHSCREEN DISPLAY KIT 11.X ENGLISH FOR USA, TOUCHSCREEN DISPLAY KIT 11.X ENGLISH, TOUCHSCREEN DISPLAY KIT 11.X GERMAN, TOUCHSCREEN DISPLAY KIT 11.X DUTCH, TOUCHSCREEN DISPLAY KIT 11.X FRENCH, TOUCHSCREEN DISPLAY KIT 11.X DANISH, TOUCHSCREEN DISPLAY KIT 11.X ESTONIAN, TOUCHSCREEN DISPLAY KIT 11.X ITALIAN, TOUCHSCREEN DISPLAY KIT 11.X NORWEGIAN. Product Usage: The GE Datex-Ohmeda Aisys Anesthesia System is intended to provide general inhalation anesthesia and ventilatory support to a wide range of patients (neonatal, pediatric, adult). The device is intended...
Source: Medical Device Recalls - November 10, 2018 Category: Medical Devices Source Type: alerts
Orthofix, Inc - Straight Plate - Class 2 Recall
Straight Plate, Sterile, Rx Only, ORTHOFIX S.r.r. Italy on label, Holes (Part Number): a) 3 Hole (003-D-01001); b) 4 Hole (003-D-02001); c) 6 Hole (003-D-03001) (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 8, 2018 Category: Medical Devices Source Type: alerts
Orthofix, Inc - LPlate - Class 2 Recall
L-Plate, Sterile, Rx Only, ORTHOFIX S.r.r. Italy on label, Left or Right (Part Number): a) Left (003-E-00001L); b) Right (003-E-00001R) (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 8, 2018 Category: Medical Devices Source Type: alerts
Orthofix, Inc - NonLocking Screw - Class 2 Recall
Non-Locking Screw, Sterile, Rx Only, ORTHOFIX S.r.r. Italy on label, Size (Part Number): a)D 3.2MM X 10MM (002-D-32010) b) D 3.2MM X 12MM (002-D-32012) c) D 3.2MM X 14MM (002-D-32014) d) D 3.2MM X 16MM (002-D-32016) e) D 3.2MM X 18MM (002-D-32018) f) D 3.2MM X 20MM (002-D-32020) g) D 3.2MM X 22MM (002-D-32022) h) D 3.2MM X 24MM (002-D-32024) i) D 3.2MM X 26MM (002-D-32026) j) D 3.2MM X 28MM (002-D-32028) k) D 3.2MM X 30MM (002-D-32030) l) D 3.2MM X 32MM (002-D-32032) m) D 3.2MM X 34MM (002-D-32034) n) D 3.2MM X 36MM (002-D-32036) o) D 3.2MM X 38MM (002-D-32038) p) D 3.2MM X 40MM (002-D-32040) q) D 3.2MM X 42MM (002-D-32042...
Source: Medical Device Recalls - June 8, 2018 Category: Medical Devices Source Type: alerts
Orthofix, Inc - Locking Screw - Class 2 Recall
Locking Screw, Sterile, Rx Only, ORTHOFIX S.r.r. Italy on label, Size (Part Number): a) D 3.2MM X 10MM (002-E-32010) b) D 3.2MM X 12MM (002-E-32012) c) D 3.2MM X 14MM (002-E-32014) d) D 3.2MM X 16MM (002-E-32016) e) D 3.2MM X 18MM (002-E-32018) f) D 3.2MM X 20MM (002-E-32020) g) D 3.2MM X 22MM (002-E-32022) h) D 3.2MM X 24MM (002-E-32024) i) D 3.2MM X 26MM (002-E-32026) j) D 3.2MM X 28MM (002-E-32028) k) D 3.2MM X 30MM (002-E-32030) l) D 3.2MM X 32MM (002-E-32032) m) D 3.2MM X 34MM (002-E-32034) n) D 3.2MM X 36MM (002-E-32036) o) D 3.2MM X 38MM (002-E-32038) p) D 3.2MM X 40MM (002-E-32040) q) D 3.2MM X 42MM (002-E-32042) r...
Source: Medical Device Recalls - June 8, 2018 Category: Medical Devices Source Type: alerts
