Mann Packing Recall of Vegetable Products Affects Whole Foods Market Stores; Grocer Issues Voluntary Recall of Multiple Products
In response to Mann Packing Co., Inc ’s recall of vegetable products, Whole Foods Market is voluntarily recalling multiple products from its stores in the United States. Mann Packing issued the recall because the vegetables may be contaminated with Listeria monocytogenes. No illnesses have been repor (Source: FDA Food Safety)
Source: FDA Food Safety - November 6, 2019 Category: Food Science Authors: FDA Source Type: alerts
Mann Packing Co., Inc. Voluntarily Recalls Vegetable Products Sold in the United States and Canada Due to Potential Health Risks
The voluntary recall is a response to a notification by the Food and Drug Administration and the Canadian Food Inspection Agency of a potential contamination with Listeria monocytogenes. (Source: FDA Food Safety)
Source: FDA Food Safety - November 4, 2019 Category: Food Science Authors: FDA Source Type: alerts
NITROGEN Gas [United States Cylinder Gas Corporation]
Updated Date: Mon, 21 Oct 2019 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - October 21, 2019 Category: Drugs & Pharmacology Source Type: alerts
OXYGEN Gas [United States Cylinder Gas Corporation]
Updated Date: Mon, 21 Oct 2019 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - October 21, 2019 Category: Drugs & Pharmacology 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: Fri, 18 Oct 2019 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - October 18, 2019 Category: Drugs & Pharmacology Source Type: alerts
Abbott Laboratories Recalls Calcilo XD ® Infant Formula
Out of an abundance of caution, Abbott has voluntarily recalled a single lot of Calcilo XD ® powder cans (13.2oz / 375g) with lot number 79696K80 in the United States and Canada due to an inconsistency in aroma and color in a small number of cans from this specific batch. (Source: FDA Food Safety)
Source: FDA Food Safety - October 9, 2019 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: Mon, 30 Sep 2019 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - September 30, 2019 Category: Drugs & Pharmacology Source Type: alerts
JFC International Inc. Issues Missing English Label and Allergy Alert on Undeclared Wheat, Soybean, and Fish (Bonito) in Futaba Sesame Hijiki Rice Seasoning
JFC International Inc. of Los Angeles, CA is voluntarily recalling a rice seasoning product because it was found to be missing the English Product Label for sale in the United States. In addition, due to the missing English label, the product has undeclared Wheat, Soybean, and Fish (Bonito) allergens. People who have allergies to wheat, soybeans, or fish (bonito) run the risk of a serious life-threatening allergic reaction if they consume the product. No illnesses have been reported to date in connection with this problem. (Source: FDA Food Alergies)
Source: FDA Food Alergies - June 5, 2019 Category: Food Science Authors: FDA Source Type: alerts
United States Bakery Issues Allergy Alert On Undeclared Milk In Naked Bread Hamburger Buns
United States Bakery of Portland, Oregon is recalling Naked Bread Hamburger Buns #NothingToHide, 8 pack, affected lot codes F6 Best By June 16th, 2018 through July 16th 2018, because it may contain undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume this product. (Source: FDA Food Alergies)
Source: FDA Food Alergies - May 24, 2019 Category: Food Science Authors: FDA Source Type: alerts
Danone North America Issues Allergy Alert and Recall for Light & Fit Greek Crunch S ’mores Flavor
Danone North America is voluntarily recalling 3,521 cases of Light& Fit ® Greek Crunch Nonfat Yogurt& Toppings S ’Mores Flavor sold in the United States with an expiration date of December 30, 2018 and UPC of 36632 03825. It was discovered that some of the toppers sold on the product contain peanuts (Source: FDA Food Alergies)
Source: FDA Food Alergies - April 27, 2019 Category: Food Science Authors: FDA Source Type: alerts
OXYGEN Gas [United States Welding, Inc.]
Updated Date: Apr 11, 2019 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - April 11, 2019 Category: Drugs & Pharmacology Source Type: alerts
NITROGEN Gas [United States Cylinder Gas Corporation]
Updated Date: Feb 14, 2019 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - February 14, 2019 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: Dec 31, 2018 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - December 31, 2018 Category: Drugs & Pharmacology Source Type: alerts
Heartware, Inc. - Ventricular Assist Device System Battery Charger - Class 2 Recall
Medtronic HeartWare Ventricular Assist HVAD System Battery Charger Model 1600US - Product Usage: The HeartWare Ventricular Assist System (HVAD) is indicated in the United States (US) and European Union (EU) for use as a bridge to cardiac transplantation (BTT) as well as an alternative to transplantation as destination therapy (DT) for patients who are at risk of death from refractory end-stage left ventricular heart failure. The HVAD Pump Controller is a microprocessor unit that controls and manages HeartWare System operation. It sends power and operating signals to the blood pump and collects information from the pump. Th...
Source: Medical Device Recalls - December 8, 2018 Category: Medical Devices Source Type: alerts
Danone North America Issues Allergy Alert and Recall for Light & Fit Greek Crunch S ’ mores Flavor
Danone North America is voluntarily recalling 3,521 cases of Light& Fit ® Greek Crunch Nonfat Yogurt& Toppings S ’ Mores Flavor sold in the United States with an expiration date of December 30, 2018 and UPC of 36632 03825. It was discovered that some of the toppers sold on the product contain peanuts and are improperly labeled. People who have an allergy to peanuts run the risk of serious or life-threatening allergic reaction if they consume this product. (Source: FDA Food Safety)
Source: FDA Food Safety - December 6, 2018 Category: Food Science Source Type: alerts
