Center for Food Safety And Applied Nutrition 2025 > 자유게시판

• 목록
• 답변
• 글쓰기
• 게시판 리스트 옵션
  • 수정
  • 삭제

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 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 items. An FDA inspection of the bakery in April 2003, decided that the agency was working under insanitary circumstances. Exposed rodent bait was observed all through the facility, together with both 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, and the FDA inspection conducted on April 10 and 11, 2003, regardless that 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 conducted in September 2001. Based upon the previous historical past of the agency and evidence obtained throughout this inspection, an undercover purchase of several bread merchandise and a dietary supplement was arranged. An intensive nutrient content material evaluation of those breads was carried out by Atlanta Center for Nutrient Analysis. A Warning Letter was issued based on incorrect nutrient content material claims, unauthorized health claims, and use of authorized health claims which had been inappropriate for the product based upon analyzed content for labeled claims. For instance, FDA analyzed 7 Grain Herb Bread, 24 ounces. Analysis revealed the calorie content material is 154% (authentic analysis) and 146% (examine analysis) of the worth declared in the nutrition info. Analysis revealed the full fat content is 246% (unique) and 240% (check) of the worth declared in the nutrition data. Analysis revealed the fiber content is 42.3% (authentic) and 57.3% (test) of the worth 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 producer so that the imported product might be properly labeled. The District's recall coordinator monitored the recall. In April 2003, Forever Cheese, Inc., Whitestone, Neuro Surge Brain Support New York, reported that the firm was recalling Mitica brand Apricot Bar, web wt. 2 ounce, imported from Spain. During a routine inspection of a retail establishment, a meals 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 degree of 1363 ppm, which weren't declared on the label.

People with a severe sensitivity to sulfites or asthmatics run the risk of a serious or life-threatening allergic response if they consume this product. The agency official agreed to initiate 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 obtained 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 truth 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 critical well being threat to diabetics and different persons who must prohibit their sugar intake. The mislabeled product was canned and labeled at the Pepsi Cola Bottling plant in Burnsville, Neuro Surge Brain Support Minnesota.