Kroger
(product distributor) and Contessa Premium Foods, Inc. (product manufacturer) are recalling 24
ounce bags of Kroger brand Meals Made Simple Shrimp Linguini, because it may contain
undeclared milk product. People who have an allergy or severe sensitivity to milk products run
the risk of serious or life-threatening allergic reaction if they consume this product.

Merrick Pet Care, Inc. of Amarillo, Texas is recalling all lots of its 10 oz “Beef Filet Squares” for Dogs and “Texas Hold’ems” pet treats because they have the potential to be contaminated with Salmonella. Salmonella can affect animals and there is risk to humans from handling contaminated pet products. People handling the treats can become infected with Salmonella, especially if they have not thoroughly washed their hands after having contact with the chews or any surfaces exposed to these products.

As a precautionary measure Goya Foods, Inc. has voluntarily recalled the Mamey Pulp product produced by COCO, S.A. of Guatemala. This product is distributed nationwide through retail stores under the Goya label.

The following statement was released by officials of Wright County Egg regarding the US Food and Drug Administration’s (FDA) on-farm records review and egg testing for Salmonella. Wright County Egg of Galt, Iowa is voluntarily recalling specific Julian dates of shell eggs produced by their farms because they have the potential to be contaminated with Salmonella. Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

Strong America Ltd. of Long Island City, NY is recalling Golden Smell brand “Dried Potato” packages with code DB35/TI02.7-2001 because they contain undeclared sulfites. People who have a severe sensitivity to sulfites run the risk of serious or life-threatening reaction if they consume this product.

Salt Lake City, UT announced today that it is conducting a voluntary nationwide recall of the company’s product sold under the name Prolatis’. Prolatis’ is conducting a voluntary recall after being informed by the Food and Drug Administration (FDA) that lab analysis has found Prolatis’ to contain Sulfoaildenafil, an analogue of Sildenafil, an FDA-approved drug used as treatment for male Erectile Dysfunction (ED), making Prolatis’ an unapproved drug. The active drug ingredient is not listed on the product label. Product manufactured prior to August 9, 2010 is included in this recall. Prolatis’ is sold nationwide in double blister packs and 40 count bottles.

Novacare LLC announced today that it is conducting a voluntary nationwide recall of products sold under the following names: Stiff Nights, Aziffa, Size Matters, Erex, Mojo, Hard Drive, Eyeful, Red Magic, Straight Up, Zotrex, Monster Excyte, WOW, Xaitrex, Verect, Prolatis, Xytamax, Maxyte, Libidinal, OMG, OMG45, and Zilex (with Golden Spear).
Novacare LLC has been informed by representatives of the Food & Drug Administration (FDA) that the products appear to contain sulfoaildenafil, an analogue of Sildenafil, an FDA-approved drug used as treatment for male Erectile Dysfunction.

– Fresh Express is voluntarily recalling 2,825 cases of Veggie Lovers Salad with a Product Code of I208 and Use-by Date of August 10, 2010 out of an abundance of caution due to a possible health risk from Listeria monocytogenes. No other Fresh Express salads are included in the recall. No illnesses have been reported in association with the recall.

Ikaria, Inc. announced today that its INOMAX® DS drug-delivery systems in
the United States are being voluntarily recalled due to the potential failure of a pressure switch which may
have an impact on the administration of INOMAX® (nitric oxide) for inhalation to patients. This potential
failure was identified by Ikaria as part of its ongoing quality monitoring and review processes. This class I
recall is being conducted with the knowledge of the U.S. Food and Drug Administration (FDA).

EZVille, Ltd. of Ronkonkoma, NY, has been informed by the US Food and Drug Administration (FDA) that FDA lab analysis of Revivexxx® Extra Strength distributed by the company was found to contain undeclared tadalafil. Tadalafil is an FDA-approved drug for the treatment of male Erectile Dysfunction (ED), making Revivexxx® Extra Strength an unapproved drug.