GFS Honey Roasted Peanuts
Reason Krispak, Inc. of Grand Rapids, MI, is recalling a small quantity of Honey Roasted Peanuts packed under the GFS label because they may contain undeclared allergen tree nuts, pecans following a supplier's recall.
Good Sense Spicy Sweet Mix recall
Recalled by Krispak Inc · Grand Rapids, MI, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Krispak, Inc. is voluntarily recalling one lot of Spicy Sweet Mix due to a potential mislabeling, resulting in undeclared allergens. Good Sense City Mix (contains: Peanut, Milk, Almond, Cashew, Soy) was labeled as Good Sense Spicy Sweet Mix (contains: Peanut, Milk, Wheat, Soy), resulting in the undeclared allergens of Almond and Cashew.
Undeclared allergens: Milk 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
Good Sense Spicy Sweet Mix, 25-oz (1lb 9oz) plastic container, UPC: 030243787178
Quantity: 315 cases (1890 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 09/06/14
Where it was sold
Michigan Ohio
FDA's distribution note: Michigan and Ohio
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, 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
- Krispak Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Oct 8, 2013
- In FDA report of
- Nov 27, 2013
- Terminated
- Apr 18, 2014
- FDA recall number
- F-0182-2014 · event 66466
- Official record
- FDA enforcement report search