California Baking Company Telera Bread (La Torta Bread), 6 pack (26 oz) and 12 pack (58 oz), plastic bags
Summary
The FDA issued a Class II for California Baking Company Telera Bread (La Torta Bread), 6 pack (26 oz) and 12 p by California Bread Co.. Reason: Undeclared allergen; milk.
Details
Source
Food Recall
External ID
F-0466-2024
Action Date
2023-12-06
Status
Terminated
Category
food
Product Description
California Baking Company Telera Bread (La Torta Bread), 6 pack (26 oz) and 12 pack (58 oz), plastic bags
Lot/Code Info: Lot numbers include the color of the kwik lok closure tag and exp. date as follows: Blue NOV04, Yellow NOV06, Tan NOV08, Red NOV10, Blue NOV11, and Yellow NOV13.
Quantity Affected: 8,959 packages
Reason for Recall
Undeclared allergen; milk
Distribution
U.S. distribution to firm within California; no foreign distribution.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-11-03
Company
Chula Vista, CA
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 18 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 (California 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 California Bread Co. have FDA actions?
This is the only FDA action we have on record for California Bread Co. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0466-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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