Granny's Fudge Gorgeous Peanut Brittle recall
Recalled by JKH Enterprises · Cascade Locks, OR, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Ingredients statement declares Unsalted Cream but does not list milk. Label has allergen advisory statement "Mfg on same equipment that processes wheat, egg, peanut & tree nut. May contain traces of soy, milk, peanuts & tree nuts".
Undeclared allergens: Milk Egg Peanut Tree nuts Soy 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
Granny's Fudge Gorgeous Peanut Brittle, net wt. 5oz. or 8 oz, packed in a clear plastic container. No UPC. Label declares "***Ingredients: Sugar, peanuts, corn syrup, butter, vanilla, baking soda***Allergy Information: Mfg on same equipment that processes wheat, egg, peanut & tree nut. May contain traces of soy, milk, peanuts & tree nuts***".
Quantity: 30 packages
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.
Made on Mar 15 21.
Where it was sold
Oregon
FDA's distribution note: distributed in Oregon only.
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, egg, peanut, tree nuts, soy, 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
- JKH Enterprises
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Apr 19, 2021
- In FDA report of
- May 12, 2021
- Terminated
- May 14, 2021
- FDA recall number
- F-0491-2021 · event 87767
- Official record
- FDA enforcement report search