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 retailer locations in the six New England states. Shaw's issued the recall as a result of the Brownies Blondie contained peanuts, which weren't 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 items. An FDA inspection of the bakery in April 2003, determined that the agency was working beneath insanitary conditions. Exposed rodent bait was noticed all through the ability, together with both processing areas. As well as, the firm didn't implement ample corrective actions following the Ohio Department of Agriculture inspection conducted on February 18, 2003, and the FDA inspection conducted on April 10 and 11, 2003, even though corrections were 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 past history of the firm and evidence obtained throughout this inspection, an undercover buy of several bread products and a dietary complement was organized. An intensive nutrient content evaluation of those breads was carried out by Atlanta Center for Nutrient Analysis. A Warning Letter was issued primarily based on incorrect nutrient content claims, unauthorized health claims, and use of authorized health claims which had been inappropriate for the product based mostly upon analyzed content for labeled claims. For Neuro Surge Product Page instance, FDA analyzed 7 Grain Herb Bread, 24 ounces. Analysis revealed the calorie content is 154% (unique analysis) and 146% (test evaluation) of the worth declared in the nutrition information. Analysis revealed the full fat content material is 246% (authentic) and 240% (check) of the worth declared within the nutrition data. Analysis revealed the fiber content is 42.3% (original) and 57.3% (verify) of the worth declared in the nutrition information.

The FDA's Baltimore District Office reported that Rhee Bros., Columbia, Maryland, issued a press release April 10, 2003, asserting a recall of Chamdel brand Korean cookies in 6.34 ounce packages. One hundred fifty 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 so 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 model Apricot Bar, internet wt. 2 ounce, imported from Spain. During a routine inspection of a retail institution, a food inspector collected a sample of the product. The brand new York State Department of Agriculture and Markets laboratory evaluation revealed the presence of sulfites, calculated as sulfur dioxide, at a level of 1363 ppm, which were not declared on the label.

People with a extreme sensitivity to sulfites or asthmatics run the risk of a serious or life-threatening allergic response if they consume this product. The firm official agreed to provoke a voluntary recall and issued a press launch. The Neuro Surge Product Page 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 received 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 were not declared on the cans. This poses a serious health risk to diabetics and different individuals who must prohibit their sugar intake. The mislabeled product was canned and labeled on the Pepsi Cola Bottling plant in Burnsville, Minnesota.