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 areas in the six New England states. Shaw's issued the recall because the Brownies Blondie contained peanuts, which weren't listed within 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, determined that the firm was operating beneath insanitary conditions. Exposed rodent bait was observed all through the ability, including each processing areas. In addition, the agency didn't implement ample corrective actions following the Ohio Department of Agriculture inspection performed on February 18, 2003, and the FDA inspection carried out on April 10 and 11, 2003, despite the fact that corrections have been promised in the course of 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 conducted in September 2001. Based upon the previous historical past of the firm and evidence obtained during this inspection, an undercover purchase of a number of bread products and a dietary complement was organized. An intensive nutrient content analysis 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 had been inappropriate focus supplement for adults the product based upon analyzed content material for labeled claims. For example, FDA analyzed 7 Grain Herb Bread, focus supplement for adults 24 ounces. Analysis revealed the calorie content is 154% (original evaluation) and 146% (test evaluation) of the worth declared in the nutrition data. Analysis revealed the overall fats content is 246% (unique) and 240% (check) of the worth declared within the nutrition data. Analysis revealed the fiber content material is 42.3% (original) and 57.3% (examine) of the worth declared in the nutrition data.

The FDA's Baltimore District Office reported that Rhee Bros., Columbia, Maryland, issued a press release April 10, 2003, announcing a recall of Chamdel brand Korean cookies in 6.34 ounce packages. A hundred and fifty components per million (ppm) in 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 could be correctly labeled. The District's recall coordinator monitored the recall. In April 2003, Forever Cheese, Inc., Whitestone, focus supplement for adults New York, reported that the agency was recalling Mitica brand Mind Guard brain health Apricot Bar, net 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 chance of a severe or life-threatening allergic response if they eat this product. The firm official agreed to initiate a voluntary recall and issued a press release. The product had been distributed in New York, New Jersey, and focus supplement for adults Connecticut. Distribution of the product was suspended till the product was correctly labeled. The FDA's Minneapolis District Office obtained discover of a recall of Mug Root Beer by the Pepsi Cola Company, Inc. The recall was initiated on February 14, 2003, and was primarily based on the truth 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 cognitive health supplement threat to diabetics and different individuals who should restrict their sugar intake. The mislabeled product was canned and labeled on the Pepsi Cola Bottling plant in Burnsville, Minnesota.

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Pub: 25 Sep 2025 19:50 UTC

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