Big Sky Chocolate Chunk Peanut Butter Chip Granola
Reason The product labeling does not list sub-ingredients which contains milk, not declared in the ingredients or contains statement.
Big Sky Chocolate Chunk Granola recall
Recalled by Suburban Bread CO. · Urbandale, IA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
The product labeling does not list sub-ingredients which contains milk, not declared in the ingredients or contains statement.
Undeclared allergen: Milk
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
Big Sky Chocolate Chunk Granola, Net Wt 14oz; UPC 02503 00475
Quantity: 3900 pouches (total)
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.
All product distributed through 11/7/2022, with a sell by date of 2/7/2023
Where it was sold
Iowa
FDA's distribution note: Distributed to retail stores in Iowa and directly to consumers.
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. The risk from an undeclared allergen is to people allergic to milk; 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
- Suburban Bread CO.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Nov 7, 2022
- In FDA report of
- Dec 14, 2022
- Terminated
- Jan 18, 2023
- FDA recall number
- F-0193-2023 · event 91131
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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