Archive for September, 2019

Dorset Cheese Voluntarily Recalled by North Atlantic and Northeast Whole Foods Market Stores Due to Possible Health Risk

September 30, 2019

In response to a recall from Consider Bardwell Farm, Whole Foods Market stores in the Northeast and North Atlantic regions are voluntarily recalling Dorset cheese because of a potential contamination of Listeria monocytogenes Go to Source

Cellect Products Inc. and Oglethorpe Ltd. Issue Voluntary Worldwide Recall of Cellect Unflavored Powder & Essentials Factor Cell Synergy Unflavored Powder, Lot #041907 Due to Potential Unsafe Levels of Arsenic and Lead

September 30, 2019

The Cellect Unflavored Powder & Essentials Factor Cell Synergy Unflavored Powder has been found to have unsafe levels of Arsenic and Lead. Go to Source

Mavidon Issues Voluntary Worldwide Recall of LemonPrep® Tubes and Single Use Cups

September 30, 2019

Mavidon is voluntarily recalling 21 lots of LemonPrep® 4 ounce tubes and single use cups to user level. These products have been found to be contaminated with Burkholderia cepacia. The specific lots are listed below: Go to Source

Consider Bardwell Farm Recalls Dorset, Slyboro, and Experience Because of Possible Health Risk

September 30, 2019

These products may be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Healthy individuals may suffer only short-term symptoms such as high fever, severe he Go to Source

Rong Shing Trading Ny Inc. Issues Allergy Alert on Undeclared Milk in Ganchi Naiweitangpian Candies

September 27, 2019

RONG SHING NY Trading Inc. of Brooklyn, NY, is recalling its 280-gram (9.8-ounce) packages of GANCHI NAIWEITANGPIAN candy because they may contain undeclared milk allergen. Consumers who are allergic to milk may run the risk of serious or life-threatening allergic reactions if they consume this prod Go to Source

Keurig Dr Pepper Announces Voluntary Withdrawal of Unflavored Peñafiel Mineral Spring Water that Does Not Meet FDA Bottled Water Quality Standards

September 26, 2019

Keurig Dr Pepper today announced it will voluntarily withdraw Peñafiel unflavored mineral spring water products, imported from Mexico, due to the presence of violative levels of arsenic. Go to Source

Weaver Fundraising, LLC Issues Allergy Alert on Undeclared Almonds, Cashews, and Pecans in Trail’s End Chocolatey Caramel Crunch Sold in Houston and Corpus Christi, Texas

September 26, 2019

Weaver Fundraising, LLC (Indianapolis, IN) is voluntarily recalling 15 oz. tins containing Trail’s End Chocolatey Caramel Crunch because they may inadvertently contain almonds, cashews and pecans. Go to Source

Apotex Corp. Issues Voluntary Nationwide Recall of Ranitidine Tablets 75mg and 150mg (All pack sizes and Formats) due to the potential for Detection of an Amount of Unexpected Impurity,N-nitrosodimethylamine (NDMA) Impurity in the product

September 25, 2019

Apotex Corp. is voluntarily, on a precautionary basis, recalling Ranitidine Tablets 75mg and 150mg (All pack sizes and Formats) to the Retail level. Apotex has learned from the U.S. Food and Drug Administration and other Global regulators that some ranitidine medicines including brand and generic fo Go to Source

Weaver Fundraising, Llc Issues Allergy Alert on Undeclared Almonds, Cashews, and Pecans in Trail’s End Chocolatey Caramel Crunch Sold in Houston and Corpus Christi, Texas

September 25, 2019

Weaver Fundraising, LLC (Indianapolis, IN) is voluntarily recalling 15 oz. tins containing Trail’s End Chocolatey Caramel Crunch because they may inadvertently contain almonds, cashews and pecans. Go to Source

B. Braun Medical Inc. Issues Voluntary Nationwide Recall of one lot of one catalog item number of an Infusomat® Space Volumetric Infusion Pump Administration Set, Due to Potential Leakage

September 24, 2019

B. Braun Medical Inc. [B. Braun] initiated a voluntary recall of one lot of Infusomat® Space Volumetric Infusion Pump Administration Sets (Catalog Number 363032, Lot Number 0061641410). The recalled administration sets are used to deliver parenteral fluids. B. Braun identified through customer compl Go to Source

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