![]() ![]() At that time, they were manufacturing Ruffles Cheddar & Sour Cream Potato Chips and intended to change the bagmaker to 1.5oz size Ruffles Cheddar & Sour Cream however, their bagmaker operator incorrectly used the Ruffles Original film. They did not implement their roll change procedure while manufacturing the recalled bags labeled “Ruffles Original Potato Chips” but containing Ruffles Cheddar & Sour Cream Potato Chips. ![]() This incorrect labeling caused their product to contain an undeclared major food allergen, milk. The firm did not adequately implement food allergen controls at the packaging step at their Vancouver, WA facility to significantly minimize or prevent the hazard of undeclared allergens when they packaged Ruffles Cheddar & Sour Cream Potato Chips in Ruffles Original bags on June 24, 2020.The firm did not identify and implement preventive controls to provide assurances that any hazard requiring a preventive control will be significantly minimized or prevented and the food manufactured, processed, packed, or held by their facility will not be adulterated, as evidenced by the following:.Hazard Analysis and Risk-Based Preventive Controls: As a result, the FDA issued an FDA Form 483. The FDA’s inspections revealed that the firm was not in compliance with the Current Good Manufacturing Practice, Hazard Analysis, and Risk-Based Preventive Controls for Human Food regulations. 29, 2020, inspection at its Vancouver, WA, manufacturing facility. 25, 2020, inspection at Frito-Lay Inc’s manufacturing facility in Bakersfield, CA, and a Sept. 24 warning letter, the FDA described a Sept. Their firm has had a total of five Class I recalls involving undeclared allergens in the past five years. The FDA inspection was triggered by a recall after a consumer complained of a bag of “Ruffles Original Potato Chips” containing “Ruffles Cheddar & Sour Cream Potato Chips.” Mislabeling and undeclared allergens can be a serious threat to public health, according to U.S. Plano, TX Frito-Lay, a food firm headquartered in Texas, is on notice from the FDA after an inspection of its manufacturing facility. ![]() The FDA frequently redacts parts of warning letters posted for public view.įrito-Lay Inc. Warning letters often are not issued until a company has been given months to years to correct problems. Business owners have 15 days to respond to FDA warning letters. Some letters are not posted for public view until weeks or months after they are sent. As part of its enforcement activities, the Food and Drug Administration sends warning letters to entities under its jurisdiction. ![]()
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