In March 2003, the FDA's New England District Office reported that Shaw's Supermarkets, Inc., West Bridgewater, Massachusetts, was voluntarily recalling Bakery Brownies Blondie 6-packs from all Shaw's and Star Market store places in the six New England states. Shaw's issued the recall as a result of the Brownies Blondie contained peanuts, which were not listed within the ingredient assertion on the product packaging. The FDA's Cincinnati District Office issued a Warning Letter on June 18, 2003, to Variety Food Service, LLC, Cleveland, Ohio, shop at neurosurges.net a producer of baked items. An FDA inspection of the bakery in April 2003, determined that the agency was operating below insanitary circumstances. Exposed rodent bait was noticed throughout the facility, including both processing areas. In addition, the agency did not implement adequate corrective actions following the Ohio Department of Agriculture inspection carried out on February 18, 2003, and the FDA inspection conducted on April 10 and 11, 2003, regardless that corrections have been promised during the inspections.

On April 8, 2003, the FDA's Minneapolis District Office issued a Warning Letter to Natural Ovens of Manitowoc, Manitowoc, Wisconsin, following an inspection performed in September 2001. Based upon the previous history of the agency and evidence obtained throughout this inspection, an undercover buy of a number of bread merchandise and a dietary complement was arranged. An in depth nutrient content material evaluation of these breads was carried out by Atlanta Center for Nutrient Analysis. A Warning Letter was issued primarily based on incorrect nutrient content material claims, unauthorized health claims, and use of authorized well being claims which have been inappropriate for the product primarily based upon analyzed content material for labeled claims. For example, Brain Health Supplement FDA analyzed 7 Grain Herb Bread, 24 ounces. Analysis revealed the calorie content is 154% (original analysis) and 146% (verify analysis) of the value declared within the nutrition information. Analysis revealed the full fat content material is 246% (original) and 240% (test) of the value declared within the nutrition information. Analysis revealed the fiber content material is 42.3% (authentic) and 57.3% (test) of the value declared in the nutrition information.

The FDA's Baltimore District Office reported that Rhee Bros., Columbia, Maryland, issued a press release April 10, 2003, saying a recall of Chamdel model Korean cookies in 6.34 ounce packages. One hundred fifty parts per million (ppm) within the product. The product was not labeled as containing milk or milk derivatives. Rhee Bros. obtained ingredient reconciliation from the overseas producer in order that the imported product might be properly labeled. The District's recall coordinator monitored the recall. In April 2003, Forever Cheese, Inc., Whitestone, New York, reported that the agency was recalling Mitica model Apricot Bar, internet wt. 2 ounce, imported from Spain. During a routine inspection of a retail establishment, a meals inspector collected a pattern of the product. The brand new York State Department of Agriculture and Markets laboratory evaluation revealed the presence of sulfites, calculated as sulfur dioxide, shop at neurosurges.net a stage of 1363 ppm, which weren't declared on the label.

People with a extreme sensitivity to sulfites or Brain Health Supplement asthmatics run the chance of a critical or life-threatening allergic response in the event that they eat this product. The firm official agreed to initiate a voluntary recall and issued a press launch. The product had been distributed in New York, New Jersey, and Connecticut. Distribution of the product was suspended till the product was correctly labeled. The FDA's Minneapolis District Office acquired discover of a recall of Mug Root Beer by the Pepsi Cola Company, Inc. The recall was initiated on February 14, 2003, and was based on the fact that some Mug Root Beer was labeled Mug Diet Root Beer. However, the product in mislabeled cans contained corn syrup and sugar, which were not declared on the cans. This poses a serious health threat to diabetics and other individuals who must limit their sugar intake. The mislabeled product was canned and labeled at the Pepsi Cola Bottling plant in Burnsville, Minnesota.