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High RiskFDAfda-F-1014-2018UNDECLARED ALLERGEN

Scotcharoo Valanga Gourmet, is a crispy rice cereal with peanut butter base, with semisweet chocolate and butterscotch melted on top. Ind...

Category
Units Affected
143
Recall Date
April 4, 2018
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1014-2018.

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.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1014-2018.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Avalanche Distributing, Llc or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1014-2018.

Avalanche Distributing, LLC

FDA

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The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

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📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

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Avalanche Distributing, Llc Recall FAQ

Avalanche Distributing, Llc is the subject of a dairy safety report: Scotcharoo Valanga Gourmet, is a crispy rice cereal with peanut butter base, with semisweet chocolate and butterscotch melted on top. Ind.... The notice was published on April 4, 2018 by the U.S. Food and Drug Administration (FDA). Approximately 143 units are potentially affected.