CPK TEQUILA LIME BASE ALLERGENS: MILK NET WEIGHT: 1 LB Case UPC FG15453558 Manufactured for California Pizza Kitchen, In
Summary
The FDA issued a Class II for CPK TEQUILA LIME BASE ALLERGENS: MILK NET WEIGHT: 1 LB Case UPC FG15453558 Manuf by Bakkavor Foods USA, Inc.. Reason: Foreign Object - Wood. The firm was notified by their supplier that the product may contain pieces of wood..
Details
Source
Food Recall
External ID
H-0098-2025
Action Date
2025-06-25
Status
Terminated
Category
food
Product Description
CPK TEQUILA LIME BASE ALLERGENS: MILK NET WEIGHT: 1 LB Case UPC FG15453558 Manufactured for California Pizza Kitchen, Inc.***Los Angeles, CA
Lot/Code Info: LOT#: 7 BEST BY: 7/5/2025, LOT#: 21 BEST BY 7/19/2025, LOT#: 27 BEST BY7/25/2025, LOT#: 30 BEST BY7/28/2025, LOT#: 31 BEST BY: 7/29/2025, LOT#: 57 BEST BY 8/24/2025
Quantity Affected: 4476/1 lb bags
Reason for Recall
Foreign Object - Wood. The firm was notified by their supplier that the product may contain pieces of wood.
Distribution
Product was shipped to the following states: AL, CA, FL & MD.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-04-10
Company
Carson, 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 56 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Bakkavor Foods USA, Inc. has 3 FDA actions in our database, including 3 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 (Bakkavor Foods USA, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Bakkavor Foods USA, Inc. have FDA actions?
Bakkavor Foods USA, 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-0098-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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