Summary
The FDA issued a Class II for Big Sky Chocolate Chunk Granola, Net Wt 14oz; UPC 02503 00475 by SUBURBAN BREAD CO.. Reason: The product labeling does not list sub-ingredients which contains milk, not declared in the ingredients or contains statement..
Details
Source
Food Recall
External ID
F-0193-2023
Action Date
2022-12-14
Status
Terminated
Category
food
Product Description
Big Sky Chocolate Chunk Granola, Net Wt 14oz; UPC 02503 00475
Lot/Code Info: All product distributed through 11/7/2022, with a sell by date of 2/7/2023
Quantity Affected: 3900 pouches (total)
Reason for Recall
The product labeling does not list sub-ingredients which contains milk, not declared in the ingredients or contains statement.
Distribution
Distributed to retail stores in Iowa and directly to consumers.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-11-07
Company
Urbandale, IA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 16 food recalls issued in the same week, part of 204 food-related FDA actions this month.
SUBURBAN BREAD CO. has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (SUBURBAN BREAD CO.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does SUBURBAN BREAD CO. have FDA actions?
SUBURBAN BREAD CO. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0193-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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