Abbott is initiating a proactive, voluntary recall of certain Similac-brand, powder infant formulas in the U.S., Puerto Rico, Guam and some countries in the Caribbean. Abott is recalling these products following an internal quality review, which detected the remote possibility of the presence of a small common beetle in the product produced in one production area in a single manufacturing facility.

House of Spices in Flushing, NY, is recalling all 10 oz. packages of Garvi Gujarat brand Tam Tam (STAR NOODLES) because they may contain undeclared peanuts. People who have an allergy to peanuts run the risk of serious or life-threatening allergic reaction if they consume this product.

Dough Masters Inc. of Troy, Michigan, is recalling all lots of their Oatmeal Raisin Cookies and Chocolate Chunk Cookies because they contain undeclared walnuts. People who have allergies to walnuts run the risk of serious or life-threatening allergic reaction if they consume these products

Hallmark Fisheries, Charleston, Ore., is recalling several packaged crab meat products because they have the potential to be contaminated with Listeria monocytogenes. Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems

Tribravus Enterprises, LLC d/b/a/ iForce Nutrition, LLC, 1305 Hot Spring Way #103, Vista CA 92081, announced today that it is conducting a voluntary nationwide recall of all Lot Codes of the company’s dietary supplement product sold under the name Reversitol, which was marketed “for promoting hormonal regulation…,” and contains 6-Etioallochol-1,4-Diene-3,17-Dione, also known as ATD, an aromatase inhibitor.

Fizogen Precision Technologies, 3133 Fortune Way, Suite #4, Wellington, FL 33414, announced today that it is conducting a voluntary nationwide recall of all Lot Codes of the company’s dietary supplement product sold under the name Off Cycle II Hardcore which contains 3,17-keto-etiochol-triene (a synonym for ATD an aromatase inhibitor). Fizogen Precision Technologies is conducting this recall after being informed by representatives of the Food and Drug Administration (FDA) that they do not believe 3,17-keto-etiochol-triene meets the definition of a dietary ingredient and therefore the product is in violation of provisions of the Food, Drug and Cosmetic Act.

Advanced Muscle Science, 4590 Deodar St., Silver Springs, Nevada 89429, announced today that it is conducting a voluntary nationwide recall of all Lot Codes of the company’s dietary supplement products sold under the names Arom-X, Arom-X UTT, Arom-XL, 4-AD, and Decavol, which are marketed as Natural Testosterone Boosters and Libido Enhancers. The products contain 1,4,6 etioallocholan-dione, also known as ATD, an aromatase inhibitor. These products are sold both individually and as part of promotional “Kits”.

Genetic Edge Technologies of Phoenix, Arizona is voluntarily recalling 60 count bottles of ArimaDex, because it may contain an Aromatase Inhibitor. Genetic Edge Technologies has been informed by the US Food and Drug Administration (FDA) that potential adverse events associated with the use of Aromatase Inhibitors could include the following: decreased rate of bone maturation and growth, decreased sperm production, infertility, aggressive behavior, adrenal insufficiency, kidney failure, and liver dysfunction.

KiloSports Inc. of Phoenix, AZ is recalling 60 Count bottles of Clomed because it may contain an Aromatase Inhibitor. KiloSports Inc. has been informed by the US Food and Drug Administration (FDA) that adverse events associated with the use of Aromatase Inhibitors could include the following: decreased rate of bone maturation and growth, decreased sperm production, infertility, aggressive behavior, adrenal insufficiency, kidney failure, and liver dysfunction.

Westmed, Inc., Tucson, AZ, is initiating a nationwide recall of 24,384 units of BagEasy Manual Resuscitation Devices. The select lots listed below of the BagEasy device have been found to have a potential for disconnection at the retention ring of the patient port manifold.