PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Allura Xper FD series and Allura Xper OR Table series - Class 2 Recall
Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the DIMMs (Dual In-line Memory Modules) used with affected systems. Allura Xper Model Name - Model Number: Allura Xper FD10 722003 722010 722026; Allura Xper FD10/10 722005 722011 722027; Allura Xper FD10C 722001; Allura Xper FD20 722006 722012 722028; Allura Xper FD20 Biplane 722008 722013; Allura Xper FD20 Biplane OR Table 722025; Allura Xper FD20 OR Table 722023 722035; Allura Xper FD20/10 722029; Allura Xper FD20/15 722058; Allura Xper FD20/20 722038; Allura Xper FD20/20 OR Table 722039; (Allura Centron - 722400 is impacted by this recall,...
Source: Medical Device Recalls - February 17, 2024 Category: Medical Devices Source Type: alerts
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Allura Xper FD series and Allura Xper OR Table series - Class 2 Recall
Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC component of affected systems. Affected PCs: Imaging Processing PC, Host PC, FlexVision PC Allura Xper Model Name - Model Number: Allura Xper FD10 722003 722010 722026; Allura Xper FD10 OR Table 722022; Allura Xper FD10/10 722005 722011 722027; Allura Xper FD10C 722001; Allura Xper FD20 722006 722012 722028; Allura Xper FD20 Biplane 722008 722013; Allura Xper FD20 Biplane OR Table 722025; Allura Xper FD20 OR Table 722023 722035; Allura Xper FD20/10 722029; Allura Xper FD20/15 722058; Allura Xper FD20/15 OR Table 722059; Al...
Source: Medical Device Recalls - February 17, 2024 Category: Medical Devices Source Type: alerts
OXYGEN gas [United States Welding, Inc.]
Updated Date: Mon, 20 Nov 2023 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - November 20, 2023 Category: Drugs & Pharmacology Source Type: alerts
NITROUS OXIDE gas [United States Welding, Inc.]
Updated Date: Mon, 20 Nov 2023 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - November 20, 2023 Category: Drugs & Pharmacology Source Type: alerts
NITROGEN gas [United States Welding, Inc.]
Updated Date: Mon, 20 Nov 2023 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - November 20, 2023 Category: Drugs & Pharmacology Source Type: alerts
UMCKA ALLERGY AND SINUS (pelargonium sidoides root, hydrastis canadensis whole, potassium chloride, sanguinaria canadensis root, pulsatilla vulgaris, silicon dioxide) tablet, chewable [Schwabe North American, Inc.]
Updated Date: Wed, 01 Nov 2023 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - November 1, 2023 Category: Drugs & Pharmacology Source Type: alerts
NITROGEN gas [United States Cylinder Gas Corporation]
Updated Date: Thu, 19 Oct 2023 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - October 19, 2023 Category: Drugs & Pharmacology Source Type: alerts
OXYGEN gas [United States Cylinder Gas Corporation]
Updated Date: Thu, 19 Oct 2023 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - October 19, 2023 Category: Drugs & Pharmacology Source Type: alerts
Unilever U.S. Voluntarily Recalls Select Knorr Sopa Soup Mix Products Due to Potential Undeclared Egg Allergen
Unilever United States Inc. is voluntarily recalling select Knorr Sopa Soup Mix products because the products may contain egg, which is not listed as an ingredient on the label. Persons who have an allergy or severe sensitivity to egg run the risk of a serious or life-threatening allergic reaction i (Source: FDA Food Alergies)
Source: FDA Food Alergies - August 10, 2023 Category: Food Science Authors: FDA Source Type: alerts
Mondel ēz Global LLC Conducts Voluntary Recall of Two Varieties of belVita Breakfast Sandwich Products Sold in the United States Due to Undeclared Peanut Allergen
Mondel ēz Global LLC announced today a voluntary recall of two varieties of belVita Breakfast Sandwich products, manufactured in the United States and sold nationwide, due to the possibility that the products may contain undeclared peanut resulting from cross-contact on a single manufacturing line. (Source: FDA Food Safety)
Source: FDA Food Safety - July 3, 2023 Category: Food Science Authors: FDA Source Type: alerts
Hu Products Issues Voluntary Allergy Alert on Undeclared Tree Nuts (Hazelnut, Cashew, and/or Almond) in Vanilla Crunch Dark Chocolate Bar Product in the U.S.
Hu Products announced today a voluntary recall in the United States of a single production lot of Vanilla Crunch Dark Chocolate Bar product (2.1 oz bar) because some packages may potentially contain undeclared hazelnut, cashew, and/or almond that were inadvertently added to the product during manufa (Source: FDA Food Alergies)
Source: FDA Food Alergies - May 18, 2023 Category: Food Science Authors: FDA Source Type: alerts
Wellness Natural USA Inc. Issues Allergy Alert on Undeclared Cashews in SimplyProtein ® Peanut Butter Chocolate Crispy Bars
Wellness Natural USA Inc. of Wilmington, DE is voluntarily recalling a single lot of its SimplyProtein ® Peanut Butter Chocolate Crispy Bar in the United States, which is sold in a 15-count variety pack that contains two other flavors, because it may contain an undeclared trace of tree nuts (cashews) (Source: FDA Food Safety)
Source: FDA Food Safety - March 31, 2023 Category: Food Science Authors: FDA Source Type: alerts
North American Food Distributing Company, Inc. Issues Allergy Alert on Undeclared Soy in 16.9 Fl Oz of Kagome Worcester Sauce and 16.9 Fl Oz of Kagome Chuno Sauce
North American Food Distributing Company, Inc of West Sacramento, Ca is recalling 16.9 fl oz of Kagome Worcester Sauce and 16.9 fl oz of Kagome Chuno Sauce, because it may contain undeclared Soy. People who have an allergy or severe sensitivity to Soy or Soy products run the risk of serious or lifet (Source: FDA Food Safety)
Source: FDA Food Safety - March 28, 2023 Category: Food Science Authors: FDA Source Type: alerts
NORTH AMERICAN CORAL SNAKE ANTIVENIN (EQUINE) (coral snake (micrurus fulvius) immune globulin antivenin (equine)) injection, powder, for solution [Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.]
Updated Date: Wed, 23 Nov 2022 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - November 23, 2022 Category: Drugs & Pharmacology Source Type: alerts
