Carefusion Recall of Alaris PC Units Model 8015 Classified as Class I Recall
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.

FDA Classifies Previous Field Action of Medtronic Surgical Device as Class I Recall
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.

Beaver Street Fisheries, Inc Voluntarily Recalls Tuna due to Possible Health Risk
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