J-Basket Brand, Napa Kimchi, Net Wt. 14.1oz. plastic jar container (12 jars per case).
Summary
The FDA issued a Class II for J-Basket Brand, Napa Kimchi, Net Wt. 14.1oz. plastic jar container (12 jars per by J F C International Inc. Reason: High levels of Yeast growth and film on top of jarred Kimchi product..
Details
Source
Food Recall
External ID
F-1752-2024
Action Date
2024-09-04
Status
Terminated
Category
food
Product Description
J-Basket Brand, Napa Kimchi, Net Wt. 14.1oz. plastic jar container (12 jars per case).
Lot/Code Info: Best Before dates: 10/26/24 and 12/19/24. UPC Code: 0 11152 83000 1
Quantity Affected: 2735 cases (case contains 12 jars)
Reason for Recall
High levels of Yeast growth and film on top of jarred Kimchi product.
Distribution
Firm ships product to the following states, WA, AZ, CO, TX, IL, NY, MD, GA, FL, HI. No foreign distribution.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-08-01
Company
Commerce, 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 24 food recalls issued in the same week, part of 204 food-related FDA actions this month.
J F C International Inc has 2 FDA actions in our database, including 2 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 (J F C International Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does J F C International Inc have FDA actions?
J F C International Inc has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1752-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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