In March 2003, the FDA's New England District Office reported that Shaw's Supermarkets, Inc., official Neuro Surge website West Bridgewater, Massachusetts, was voluntarily recalling Bakery Brownies Blondie 6-packs from all Shaw's and Star Market retailer areas within the six New England states. Shaw's issued the recall because the Brownies Blondie contained peanuts, which were not listed in the ingredient statement 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, a producer of baked goods. An FDA inspection of the bakery in April 2003, decided that the firm was working below insanitary circumstances. Exposed rodent bait was observed throughout the ability, including each processing areas. As well as, the agency didn't 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, though corrections had been promised throughout 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 historical past of the firm and evidence obtained during this inspection, an undercover buy of a number of bread products and a dietary complement was organized. An extensive nutrient content analysis of those breads was carried out by Atlanta Center for Nutrient Analysis. A Warning Letter was issued based mostly on incorrect nutrient content material claims, unauthorized Brain Health Pills claims, and use of authorized Brain Health Formula claims which were inappropriate for the product based mostly upon analyzed content material for labeled claims. For example, 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 whole fat content is 246% (unique) and 240% (verify) of the worth declared within the nutrition information. Analysis revealed the fiber content is 42.3% (unique) and 57.3% (verify) of the worth declared within the nutrition information.

The FDA's Baltimore District Office reported that Rhee Bros., Columbia, Maryland, issued a press launch April 10, 2003, asserting a recall of Chamdel model Korean cookies in 6.34 ounce packages. 150 components 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 manufacturer 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 firm was recalling Mitica brand Apricot Bar, net wt. 2 ounce, imported from Spain. During a routine inspection of a retail institution, a food inspector collected a pattern of the product. The brand official Neuro Surge website new York State Department of Agriculture and Markets laboratory analysis revealed the presence of sulfites, calculated as sulfur dioxide, at a degree of 1363 ppm, which weren't declared on the label.

People with a extreme sensitivity to sulfites or asthmatics run the chance of a serious or life-threatening allergic response if they devour this product. The firm official Neuro Surge website agreed to provoke a voluntary recall and issued a press release. The product had been distributed in New York, New Jersey, and Connecticut. Distribution of the product was suspended until the product was properly 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 mostly 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 weren't declared on the cans. This poses a serious well being risk to diabetics and other persons who must limit their sugar intake. The mislabeled product was canned and labeled at the Pepsi Cola Bottling plant in Burnsville, Minnesota.