Orval Kent announced today that it is voluntarily recalling 23 products as a precautionary measure because the products may be contaminated with Salmonella. The Orval Kent products are being recalled because they contain fresh cilantro produced and distributed by EpicVeg, Inc. of Lompoc, CA. Epic Veg, Inc. issued the notice to recall one lot of cilantro with the UPC code 033383801049 and lot 6127R on November 3, 2010.

JACKSON, Miss. (November 5, 2010)  Cal-Maine Foods, Inc. (NASDAQ: CALM) today was notified by the Food & Drug Administration (FDA) that one of the Company’s suppliers, Ohio Fresh Eggs, LLC, Croton, Ohio, had a routine environmental study sample which tested positive for Salmonella Enteritidis (SE). Cal-Maine purchased approximately 24,000 dozen unprocessed eggs from Ohio Fresh which were processed and re-packaged by the Company’s Green Forest, Arkansas, facility between October 9 and 12, 2010, yet the Company was only notified today.

Baugher Enterprise, Inc, of Westminster, Maryland, is recalling all production of Baugher’s Apple Cider because it may be contaminated with Escherichia coli O157:H7 bacteria (E. Coli O157:H7). E. coli O157:H7 causes a diarrheal illness often with bloody stools.

CareFusion (NYSE: CFN), a leading global medical device company, issued the following update regarding its previously disclosed recall of approximately 17,000 Alaris® PC units model 8015 manufactured or serviced between December 2008 and September 2009. The FDA has classified this action as a Class I recall.

WalkMed Infusion LLC, Englewood, Colorado, is initiating a nationwide recall of a total of 2018 Triton Pole Mount Infusion Pumps. The pumps have been found to possibly have a problem with the pump door open alarm, which potentially could result in over infusion of medication.

The Maryland Department of Health and Mental Hygiene (DHMH) and local health departments are conducting an investigation of a cluster of seven E. coli O157 infections. There have been no deaths, although three of the seven cases have been hospitalized. A potential association exists with the consumption of unpasteurized Baugher’s apple cider.

Further to its previously announced voluntary recall of 18 lots of Fentanyl Transdermal System 25 mcg/hour C-II patches, Actavis is encouraging consumers to return any product in their possession from the October 21, 2010 recall.

Beaver Street Fisheries, Inc. of Jacksonville, FL is recalling 5-7 lb Tuna Loins Lot 928378, because they have the potential to be contaminated with elevated levels of histamine. High levels of histamine can produce an allergic reaction called scombroid poisoning when the fish is consumed

Intelli Health Products, announced today that it is conducting a voluntary nationwide recall of Duro Extend Capsules For Men. Intelli Health Products, is conducting this recall after being informed by representatives of the Food and Drug Administration (FDA) that laboratory analysis of Duro Extend Capsules For Men sample found the product to be adulterated with Sulfoaidenafil, an analogue of sildenafil which is an FDA approved drug used in the treatment of Erectile Dysfunction(ED), making it an unapproved new drug.

Medtronic, Inc. (NYSE: MDT) today announced the U.S. Food and Drug Administration (FDA) has classified the company’s previous action related to the Octopus® Nuvo Tissue Stabilizer as a Class I recall. FDA classifies a recall as Class I when the agency believes that there is a reasonable probability that use of the recalled product will cause serious adverse health consequences or death.