Ultimate Chocolate Chip Cookie Dough Pie
Reason Product incorporated cookie dough that was potentially contaminated with Listeria Monocytogenes.
9" French Silk Base recall
Recalled by American Blue Ribbon Holdings LLC · Chaska, MN, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Undeclared Pecan
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
9" French Silk Base, Item 7545, Count per case 6 Ea., Case Weight 12 lb. 3 oz. UPC 50796220075458. Keep Frozen.
Quantity: 390 Cases (6 pies per case)
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 Code Printed on the side of the pie tin: CH20322CPS (Hour)(Minute) 7545 Case Label CH20326FSK
Where it was sold
Arkansas Arizona Iowa Illinois Kansas Minnesota Missouri North Dakota Nebraska Oklahoma Wyoming
FDA's distribution note: Pies shipped to two distributors who shipped to Village Inn Restaurants located in the following states: AR, AZ, IA, IL, KS, MN, MO, ND, NE, OK, and WY.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. 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
- American Blue Ribbon Holdings LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 22, 2020
- In FDA report of
- Jan 13, 2021
- Terminated
- Feb 5, 2021
- FDA recall number
- F-0200-2021 · event 87045
- Official record
- FDA enforcement report search