Pompano Beach, FL –Atlas Operations, Inc. announced today that it is expanding its December 12, 2009 voluntary nationwide recall of the company’s dietary supplements for sexual enhancement to include Stamin It, Erectzia, and Vigor 100.
Response Products Voluntarily Recalls Advanced Cetyl M Joint Action Formula for Dogs Because of Possible Salmonella Health Risk
Response Products, Broken Bow, NE is voluntarily recalling Cetyl M for Dogs, lot numbers 1210903 and 0128010, due to a possible Salmonella contamination from the hydrolyzed vegetable protein component provided by Basic Foods of Las Vegas, NV. Tests conducted by Basic Foods to detect Salmonella produced negative results; however, Response Products has determined to recall the above-referenced lots.
Consumer Alert Precautionary Recall issued for H-E-B French Onion Dip
H-E-B, committed to the safety of customers, is issuing a precautionary recall for H-E-B French Onion Dip. H-E-B is expanding the recall announced Thursday. In addition to the product with code dates of 4/15/2010 and 4/20/2010, new affected code dates are 4/23/2010 and 4/24/2010 in the 8 ounce, 16 ounce and 24 ounce sizes.
Mccormick & Company Recalls Mccormick Fajitas Seasoning Mix Due To Unlabeled Wheat And Milk Ingredients
McCormick & Company, Incorporated (NYSE:MKC) has announced a voluntary recall of McCormick Fajitas Seasoning Mix, with UPC Code 5210002121 and “BEST BY” dates of JAN 16 12 AH and JAN 16 12 CH. McCormick Fajitas Seasoning Mix packages with these date codes contain undeclared wheat and milk ingredients.
Podcast for Healthcare Professionals: Ongoing Safety Review of Stalevo (entacapone/carbidopa/levodopa) and possible development of Prostate Cancer
Update about an ongoing safety review of Stalevo and an increased risk for developing prostate cancer.
US Oftalmi Announces Voluntary Recall of the Camolyn Eye Drops Product Line, and Fisiolin Nasal Drops. Includes All Lots of 15mL Bottles.
US Oftalmi, of Hallandale, Florida, announced today that it is conducting a voluntary nationwide recall of all Over-the-Counter Eye Drops and Nasal Drops. Products are packaged in 15mL plastic bottles and were distributed nationwide to food and drug distributors for retail.
Del Bueno Amends Recall of Queso Fresco Cheese Because of Possible Health Risk
Del Bueno of Grandview, WA is recalling all size packages of Queso Fresco Fresh Cheese because it has the potential to 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. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
Del Bueno Recalls Queso Fresco Because of Possible Health Risk
Del Bueno of Grandview, WA is recalling 16oz. packages of Queso Fresco Fresh Cheese because it has the potential to 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. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
Kroger Recalls Two Seasonings Due to Possible Health Risk
The Kroger Co. said today it is recalling Kroger California Seasoning Blend Garlic Powder and Kroger Special Seasoning Blend Lemon Pepper sold in its retail stores because the Company has been made aware by a supplier that an ingredient in the product may have been contaminated with Salmonella.
Kanec USA Inc., Issues a Voluntary Nationwide Recall of Stud Capsule For Men Marketed as Dietary Supplements
KANEC USA INC, 5061, South State Road 7.
Ste 602, Davie FL 33314, announced today that it is conducting a voluntary nationwide recall of Stud Capsule For Men Lot #060607-01/060108-01 Exp 6-2013. Kanec USA Inc, is conducting this recall after being informed by representatives of the the Food and Drug Administration (FDA) that laboratory analysis of Stud Capsule Lot 060607-01/060108-01 Exp 6-2013 sample found the product to be adulterated with Sildenafil , an FDA approved drug used in the treatment of Erectile Dysfunction(ED).