Momchipz Gluten Free Veggie Chips Broccoli Florets & Cauliflower
Reason Undeclared Wheat.
Potter's Crackers Classic White recall
Recalled by Potters Fine Foods, LLC · Madison, WI, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Potters Fine Foods LLC are recalling Potter's Crackers Classic White because of cross contamination with a Basil Walnut Presto Cracker dough. Even though there is an allergen statement on the Classic White tag for tree nuts, we initiated a voluntary recall. All 109 packages were accounted for.
Undeclared allergen: Tree nuts
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
Potter's Crackers, Classic White, Net Wt 5 ounces, UPC 6 80569 15877 2, Potters Fine Foods LLC, 100 S. Baldwin, Madison WI 53703., Ingredients, Wheat Flour, Milk, Butter, Cracked Wheat, Sugar, Crystal Salt, Baking Powder, Black Pepper. Allergen Information: wheat, dairy & tree nuts.
Quantity: 109 containers.
Food: Chips & snacks
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
10-10-13
Where it was sold
Illinois North Carolina New York Wisconsin
FDA's distribution note: IL, NY, NC, WI.
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. The risk from an undeclared allergen is to people allergic to tree nuts; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Potters Fine Foods, LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 9, 2013
- In FDA report of
- Sep 11, 2013
- Terminated
- Apr 17, 2015
- FDA recall number
- F-1868-2013 · event 66018
- Official record
- FDA enforcement report search
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