Bread and Roll Mix; 50 lb. multi-wall, kraft, poly-lined moisture proof bags
Summary
The FDA issued a Class I for Bread and Roll Mix; 50 lb. multi-wall, kraft, poly-lined moisture proof bags by B.C. Williams Bakery Service, Inc. Reason: Undeclared Milk Allergen.
Details
Source
Food Recall
External ID
H-0500-2026
Action Date
2026-02-11
Status
Ongoing
Category
food
Product Description
Bread and Roll Mix; 50 lb. multi-wall, kraft, poly-lined moisture proof bags
Lot/Code Info: Lot #072225-217 Lot #072225-218 Lot #080325-200 Lot #080325-201 Lot #081625-203 Lot #081625-204 Lot #092225-222 Lot #092225-223 Lot #092225-224 Lot #092225-225 Lot #092225-226 Lot #092225-227 Lot #092225-228 Lot #101725-208 Lot #101725-209
Quantity Affected: 720 Bags
Reason for Recall
Undeclared Milk Allergen
Distribution
Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2025-12-23
Company
Dallas, TX
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 69 food recalls issued in the same week, part of 204 food-related FDA actions this month.
B.C. Williams Bakery Service, Inc has 3 FDA actions in our database, including 3 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (B.C. Williams Bakery Service, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does B.C. Williams Bakery Service, Inc have FDA actions?
B.C. Williams Bakery Service, Inc has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0500-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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