As of December 2, 2014, a total of 87 people infected with the outbreak strains of Salmonella Enteritidis have been reported from 11 states.

Twenty-seven percent of ill persons have been hospitalized. No deaths have been reported.

CDC’s National Antimicrobial Resistance Monitoring System (NARMS) laboratory conducted antibiotic resistance testing on Salmonella Enteritidis isolates collected from

Overhill Farms, Inc. of Vernon, California is voluntarily recalling the frozen food product Open Nature Chile Cheese Enchiladas due to potential Salmonella contamination. The supplier for the organic cilantro contained in such product notified Overhill Farms that the organic cilantro may have Salmonella contamination based on routine testing conducted. The product is sold nationwide at

As of November 24, a total of 68 persons infected with the outbreak strains of Salmonella have been reported from 10 states. The number of ill people identified in each state is as follows: Connecticut (4), Maine (3), Massachusetts (31), Montana (1), New Hampshire (4), New York (5), Ohio (1), Pennsylvania (10), Rhode Island (6),

Time for a Warning?

Three people in Vermont and four people in New Hampshire have been sickened by Salmonella believed to be associated with bean sprouts, health officials in the two states said Friday.

According to the Vermont Department of Health, the Centers for Disease Control reported Friday (not yet on its website) that

Boston’s Fox 25 News reports that Massachusetts state and federal health officials are looking into cases of salmonella that have been reported in multiple states.

The Massachusetts Department of Health confirmed on Thursday afternoon that the agency, along with the Centers for Disease Control and Food and Drug Administration, are investigating a potential multi-state salmonella

Coral Beach of the Packer reports this morning that positive test results for salmonella contamination spurred Latin Specialties Inc., Houston, to recall 80 cases of whole avocados from Unity Groves Corp. in Florida.

The Houston company initiated the voluntary recall Oct. 30, according to a Nov. 19 enforcement report from the Food and Drug Administration.