Stemvida International Corporation of Ontario California is recalling StemAlive 90 Capsules, because it contains undeclared milk. People who have an allergy or severe sensitivity to milk (bovine colostrum) run the risk of serious or life-threatening allergic reaction if they consume this product.
Category Archives: Food & Drug Recalls
FDA Commissioner Margaret A. Hamburg’s Statement on the 50th Anniversary Surgeon General’s Report on Smoking and Health
The 50th anniversary of the release of the Surgeon General’s Report on Smoking and Health is an opportunity to reflect on the important progress that has been made in tobacco control and to look ahead on addressing this critical public health issue. In 2014, tobacco remains the leading preventable cause of disease and death in this country. For five decades, the Department of Human Health and Services has played a critical role in developing and implementing proven comprehensive tobacco control programs and policies aimed at preventing tobacco use, especially among youth, and encouraging cessation. The Surgeon General’s Report provides a scientific foundation for public health action to reduce the public health impact of tobacco use.
FDA allows marketing for first of-its-kind post-natal test to help diagnose developmental delays and intellectual disabilities in children
Today the U.S. Food and Drug Administration authorized for marketing the Affymetrix CytoScan Dx Assay, which can detect chromosomal variations that may be responsible for a child’s developmental delay or intellectual disability. Based on a blood sample, the test can analyze the entire genome at one time and detect large and small chromosomal changes.
The Mentholatum Company Issues Voluntary Nationwide Recall of Rohto® Eye Drops Made in Vietnam
The Mentholatum Company announced today it is conducting a voluntary recall to the retail level of Rohto® Arctic, Rohto® Ice, Rohto® Hydra, Rohto® Relief and Rohto® Cool eye drops Made in Vietnam. This recall includes ONLY lots of product that were manufactured in Vietnam and DOES NOT include eye drops made in Japan.
Paskesz Candy Company Issues Allergy Alert on Undeclared Milk in Premium Belgian Chocolate Coins
Paskesz Candy Company, Brooklyn, New York is recalling its Premium Belgian Chocolate Coins Hologram .5 oz bags because they may contain traces of milk. People who have allergies to milk run the risk of serious or life-threatening allergic reaction if they consume these products.
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Tandem Diabetes Care Initiates Voluntary Recall for Specific Lots of Insulin Cartridges Used with t:slim Insulin Pump
andem Diabetes Care®, Inc. (NASDAQ: TNDM) today announced that it is initiating a voluntary recall of specific lots of insulin cartridges that are used with the t:slim® Insulin Pump. The affected cartridges may be at risk for leaking.
Human Science Foundation Issues Voluntary Nationwide Recall of Pro ArthMax Due to Undeclared Active Pharmaceutical Ingredients
Jan 13, 2014 – Gardena, CA, Human Science Foundation is voluntarily recalling all lots of Pro ArthMax 120 count bottle, labeled and sold as a dietary supplement to the consumer level. The product has been found to contain undeclared active pharmaceutical ingredients (APIs), making it an unapproved new drug.
Allergy Alert – Undeclared Milk in Five Kinnikinnick Foods Products
Kinnikinnick Foods of 10940 120 street, Edmonton, AB is warning consumers with MILK Allergies not to consume the following Kinnikinnick Products: Original Homestyle Waffles,
Cinnamon & Brown Sugar Homestyle Waffles, Pancake & Waffle Mix, Kinni-Kwik Bread & Bun Mix, Panko Style Bread Crumbs.
FDA approves Mekinist in combination with Tafinlar for advanced melanoma
This week the U.S. Food and Drug Administration approved Mekinist (trametinib) in combination with Tafinlar (dabrafenib) to treat patients with advanced melanoma that is unresectable (cannot be removed by surgery) or metastatic (late-stage).
Midwest Wholesale Issues Voluntary Recall of Boost Ultra, XZone Gold, Sexy Monkey, Triple MiracleZen Platinum, Magic for Men, "New" Extenze, and New XZen Platinum Marketed as a Dietary Supplements Due to the Presence of Undeclared Drug Ingredients
Nixa, MO, Midwest Wholesale is voluntarily recalling the following products and Lot numbers. This recall is being conducted to the consumer level. FDA analysis found these products to contain undeclared Sildenafil and/or Tadalafil, the active ingredients in FDA-approved prescription drugs used to treat erectile dysfunction (ED).