Valanga Gourmet brand Snickerdoodle Cookie with cinnamon sugar on the outside
Reason The firm declares whey as the margarine's sub-ingredient but does not declare milk.
Scotcharoo Valanga Gourmet recall
Recalled by Avalanche Distributing, LLC · Zillah, WA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Scotcharoo product is recalled because the Contains statement does not declare Milk and Soy. Whey, Milk, and Soy Lecithin are declared in the Ingredients statement.
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
Scotcharoo Valanga Gourmet, is a crispy rice cereal with peanut butter base, with semisweet chocolate and butterscotch melted on top. Individually wrapped, sold in boxes of 12. Net Wt. 3.2 oz (91g). UPC 814524611556. The product label is read in parts: "***VALANGA GOURMET Scotcharoo***Ingredients: Peanut Butter ***Semi-sweet Chocolate (Sguar, Chocolate, Milkfat, Cocoa Butter, Soy Lecithin, Natural Flavors***Butterscotch Chips (Sugar, Palm Kernel and Palm Oils, Whey, Nonfat Milk, Natural Flavor, Added Color, Sunflower, Lecithin, and Vanilla) ***Contains Peanuts***".
Quantity: 143 boxes (12 counts per box)
Food: Pasta, rice & grains
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.
No Lot number or Expiration Date on package
Where it was sold
Oregon Washington
FDA's distribution note: distributed in OR and WA
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
- Avalanche Distributing, LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Apr 4, 2018
- In FDA report of
- Apr 25, 2018
- Terminated
- May 9, 2018
- FDA recall number
- F-1014-2018 · event 79737
- Official record
- FDA enforcement report search
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