UPC 24144500000 Ready Meals PEANUT BUTTER CHOCOLATE CHIP BAR With…
Reason Contains statement does not declare Almond
Barricini Milk Chocolate Peanut Butter Pretzels in recall
Recalled by Bazzini Holdings L.L.C. · Allentown, PA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Undeclared wheat. The back panel applied to some containers of milk chocolate peanut butter pretzels was for milk chocolate peanut butter cups, which does not declare wheat.
Undeclared allergens: Milk Peanut Wheat
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
Barricini Milk Chocolate Peanut Butter Pretzels in Net Wt 6.5 oz. plastic tub, UPC 075655235181 Back Panel: Milk Chocolate Peanut Butter Cups Barricini Manufactured by Bazzini Holdings, LLC Allentown, PA 18106
Quantity: 1000 cases, 12,000 units
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.
Lot 1E083
Where it was sold
Nationwide.
FDA's distribution note: Nationwide, excluding Pacific States
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to milk, peanut, wheat; 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
- Bazzini Holdings L.L.C.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 2, 2014
- In FDA report of
- Jul 16, 2014
- Terminated
- Aug 18, 2015
- FDA recall number
- F-2171-2014 · event 68316
- Official record
- FDA enforcement report search
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