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 locations 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 manufacturer of baked items. An FDA inspection of the bakery in April 2003, determined that the agency was operating underneath insanitary circumstances. Exposed rodent bait was noticed all through the ability, together with each processing areas. As well as, the agency did not implement enough corrective actions following the Ohio Department of Agriculture inspection conducted on February 18, 2003, Brain Health Formula Brain Health Support Pills and the FDA inspection carried out on April 10 and 11, 2003, despite the fact that corrections were promised in the course of the inspections.

On April 8, 2003, the FDA's Minneapolis District Office issued a Warning Letter to natural brain support supplement Ovens of Manitowoc, Manitowoc, Wisconsin, natural brain support supplement following an inspection conducted in September 2001. Based upon the previous historical past of the firm and evidence obtained throughout this inspection, an undercover buy of several bread products and a dietary complement was arranged. An in depth nutrient content 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 Brain Health Formula claims, and use of authorized well being 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 material is 154% (unique evaluation) and 146% (test evaluation) of the value declared in the nutrition data. Analysis revealed the full fats content material is 246% (unique) and 240% (test) of the worth declared in the nutrition data. Analysis revealed the fiber content is 42.3% (unique) and 57.3% (test) of the value declared in the nutrition info.

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) in 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 may very well be correctly labeled. The District's recall coordinator monitored the recall. In April 2003, Forever Cheese, Inc., Brain Health Support Brain Health Supplement Pills Whitestone, New York, reported that the firm was recalling Mitica model Apricot Bar, natural brain support supplement web wt. 2 ounce, imported from Spain. During a routine inspection of a retail establishment, natural brain support supplement a food 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, at a stage of 1363 ppm, natural brain support supplement which weren't declared on the label.

People with a extreme sensitivity to sulfites or asthmatics run the risk of a critical or life-threatening allergic reaction in the event that they devour 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 until the product was properly labeled. The FDA's Minneapolis District Office acquired notice 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, natural brain support supplement which weren't declared on the cans. This poses a severe well being risk to diabetics and different individuals who must restrict their sugar intake. The mislabeled product was canned and labeled on the Pepsi Cola Bottling plant in Burnsville, Minnesota.