Top Label: TRADER JOE'S GENOVA PESTO NET WT. 7 OZ. (198g) Side Label: TRADER JOE'S HUMMUS DIP NET WT. 7 OZ (98g) CONTAIN
Summary
The FDA issued a Class II for Top Label: TRADER JOE'S GENOVA PESTO NET WT. 7 OZ. (198g) Side Label: TRADER JOE by Bakkavor Foods USA Inc.. Reason: The firm was notified that the product top label reads "Pesto" and the side label reads "Hummus". The Hummus ingredient panel does not include milk an.
Details
Source
Food Recall
External ID
F-0894-2023
Action Date
2023-05-24
Status
Terminated
Category
food
Product Description
Top Label: TRADER JOE'S GENOVA PESTO NET WT. 7 OZ. (198g) Side Label: TRADER JOE'S HUMMUS DIP NET WT. 7 OZ (98g) CONTAINS: SESAME. DIST. & SOLD EXCLUSIVELY BY: TRADER JOE'S, MONROVIA, CA 91016 UPC 0015 7353
Lot/Code Info: BEST BY 5/27/2023 Time stamp between 06:28 - 07:07 Top label: SKU 15739 Side label: SKU 15735
Quantity Affected: 290cs/24/7 oz cups
Reason for Recall
The firm was notified that the product top label reads "Pesto" and the side label reads "Hummus". The Hummus ingredient panel does not include milk and walnuts which are ingredients of the Pesto in the container.
Distribution
Product was shipped to the following states: AZ, CA, FL & WA.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-05-01
Company
Charlotte, NC
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 74 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 "F-0894-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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