Charles Products, Inc. (CPI) announced today that it is voluntarily recalling shot and pint glasses identified below sold exclusively through M&M’S World retail stores in New York, Las Vegas, Orlando and London.
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Category Archives: Food & Drug Recalls
United States enters consent decree with New York dietary supplement manufacturer
Triceutical, Inc., of Farmingdale, New York, and Liqun Zhang, the company’s president, have agreed to stop production and distribution of dietary supplements under the terms of a consent decree because of violations of federal dietary supplement regulations, known as Current Good Manufacturing Practice (cGMP) requirements.
Whole Foods Market Recalls Pre-packaged Mini Caesar And Mini Mesclun Goat Cheese Salad In Three States, Due To Undeclared Allergen
Whole Foods Market is recalling mini 4oz. containers of pre-packaged Caesar salad and Mesclun Goat Cheese salad sold in stores on July 8,, 2014 throughout New York, New Jersey (Excluding Princeton, Cherry Hill and Marlton) and Connecticut (Excluding Glastonbury, West Hartford and Bishop’s Corner) due to mislabeling and a resulting undeclared allergen of fish and egg (Caesar) and tree nuts (Mesclun Goat Cheese). The product has a Sell by date of: 7/11/14.
Vascular Solutions, Inc. Issues Recall of Langston Dual Lumen Catheters
Vascular Solutions, Inc. initiated a voluntary nationwide recall of Langston dual lumen catheters used in catheterization procedures. The Langston dual lumen catheter is indicated for delivery of contrast medium in angiographic studies and for simultaneous pressure measurement from two sites.
FDA Classifies ConvaTec’s Voluntary Global Recall of Flexi-Seal™ CONTROL Fecal Management System (FMS) as Class I
ConvaTec has announced that the U.S. Food and Drug Administration (FDA) has classified the company’s recently initiated voluntary global recall of Flexi-Seal™ CONTROL Fecal Management System (FMS) as a Class I recall.
FDA approves Beleodaq to treat rare, aggressive form of non-Hodgkin lymphoma
The U.S. Food and Drug Administration today approved Beleodaq (belinostat) for the treatment of patients with peripheral T-cell lymphoma (PTCL), a rare and fast-growing type of non-Hodgkin lymphoma (NHL). The action was taken under the agency’s accelerated approval program.
Cargill Conducts Voluntary Recall of Select Nutrena® NatureWise® Meatbird Feed Due to Possible Animal Health Risk
Minneapolis, Minn., – 1 July 2014 – Cargill’s animal nutrition business today announced a voluntary recall of its Nutrena NatureWise meatbird feed due to excess levels of sodium. Sodium is an essential nutrient for poultry.
Federal judge approves consent decree with New York dietary supplement maker
A federal judge in New York has signed a consent decree for permanent injunction between the United States and Mira Health Products Ltd., a dietary supplement manufacturer located in Farmingdale, New York, and Michael S. Ragno and Michael S. Ragno, Jr.
Oriya Organics, LLC Voluntarily Recalls Oriya Organics Superfood Protein Medley Containing Sprouted Chia Seed Powder for Possible Salmonella Contamination
Oriya Organics, LLC is voluntarily recalling Oriya Organics Superfood Protein Medley which contain Organic Sprouted Chia Seed Powder due to possible health risks related to Salmonella contamination.
FDA seeks permanent injunction against California pharmaceutical company
On June 25, the U.S. Department of Justice, at the request of the U.S. Food and Drug Administration, filed a complaint for permanent injunction in the U.S. District Court for the Central District of California against Laclede, Inc. (Laclede) of Rancho Dominguez, California, and its president, Michael A. Pellico. The complaint claims that Laclede illegally distributes over-the-counter vaginal drug products without required FDA approval.