So Delicious Dairy Free Salted Caramel Cluster Cashewmilk
Reason Product may contain foreign material: small stones and other hard objects.
Fannie May Pixies recall
Recalled by Fannie May Confections Brands, Inc · Maple Heights, OH, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
The products outer holiday wrap has an information panel that is incorrect. The information panel does not declare that pecans are in product. The actual box under wrapping correctly declares that pecans are in the product.
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
Fannie May Pixies , Caramel and Pecan Clusters covered in Milk Chocolate 14 oz. Box - 12 units per case
Quantity: 173,076 boxes (14 oz.) Pixies
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 numbers: 17352 1, 18262 2, 18263 2, 18291 1, 18291 2, 18293 2, 18295 2, 18298 2,18303 1, 18303 2, 18304 2, 18305 1, 18305 2, 18306 2, 18307 1, 18307 2, 18309 2,18310 1, 18310 2, 18311 2, 18312 2, 18313 2, 18316 1, 18316 2, 18317 2, 18318 1,18318 2, 18330 2, 18331 1
Where it was sold
Alabama Florida Illinois Indiana Kentucky Minnesota Pennsylvania Texas Washington Wisconsin
FDA's distribution note: The product at issue was distributed to customers in 10 states. IL, WI, IN,MN, WA, TX, PA, AL, KY, FL
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
- Fannie May Confections Brands, Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 18, 2018
- In FDA report of
- May 8, 2019
- Terminated
- Apr 28, 2020
- FDA recall number
- F-1315-2019 · event 81856
- Official record
- FDA enforcement report search
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