Blue Oven Artisan Bakery English Muffins, Net Wt. 13.4 oz (380g), packaged as a 4-pack in a clear plastic bag, UPC 19871
Summary
The FDA issued a Class II for Blue Oven Artisan Bakery English Muffins, Net Wt. 13.4 oz (380g), packaged as a by Blue Oven Bakery, Inc.. Reason: Undeclared allergen - milk.
Details
Source
Food Recall
External ID
H-0173-2026
Action Date
2025-11-19
Status
Terminated
Category
food
Product Description
Blue Oven Artisan Bakery English Muffins, Net Wt. 13.4 oz (380g), packaged as a 4-pack in a clear plastic bag, UPC 198715684322
Lot/Code Info: No codes applied, but customers receive a copy of the order sheet with the production date listed.
Quantity Affected: ~4,500 bags
Reason for Recall
Undeclared allergen - milk
Distribution
Product distributed to 5 retailers in IN, KY, and OH
Type: Voluntary: Firm initiated
Recall Initiated: 2025-10-30
Company
Cincinnati, OH
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 44 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (Blue Oven Bakery, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Blue Oven Bakery, Inc. have FDA actions?
This is the only FDA action we have on record for Blue Oven Bakery, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0173-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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