So Delicious Dairy Free Salted Caramel Cluster Cashewmilk
Reason Product may contain foreign material: small stones and other hard objects.
Libby's Gourmet Desserts brand pecan pie recall
Recalled by Libby's Gourmet Desserts · Cincinnati, OH, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
No ingredient Statement on box. Labeled incorrectly. Product is being recalled because there is no ingredient statement on the box. Product contains multiple allergen ingredients.
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
Libby's Gourmet Desserts brand pecan pie. Pies placed in metal pie tins which are then put in a cardboard sleeve with plastic wrapping
Quantity: 696
Food: Nuts & seeds Bread & bakery
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.
Codes are Julian Calendar dates stamped on the pies on their date of manufacture, in the form: mm/dd/year. Recalled product coded 01/01/2012 through 07/17/2012.
Where it was sold
Kentucky Ohio
FDA's distribution note: Distributed within the US to two wholesalers/distributors located in the states of Ohio and Kentucky. There are no government, Canadian, or Foreign consignees
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. 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
- Libby's Gourmet Desserts
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 17, 2012
- In FDA report of
- Aug 29, 2012
- Terminated
- Mar 1, 2013
- FDA recall number
- F-1951-2012 · event 62688
- Official record
- FDA enforcement report search
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