Ziyad Brand Jameed Soup Starter sold in a 35.2 fluid ounce tetra pak container with UPC code 0 74265 00597 1. 12 units
Summary
The FDA issued a Class II for Ziyad Brand Jameed Soup Starter sold in a 35.2 fluid ounce tetra pak container w by ZB Importing LLC. Reason: Does not declare the major food allergen "milk".
Details
Source
Food Recall
External ID
F-1305-2023
Action Date
2023-08-09
Status
Terminated
Category
food
Product Description
Ziyad Brand Jameed Soup Starter sold in a 35.2 fluid ounce tetra pak container with UPC code 0 74265 00597 1. 12 units per wholesale case
Lot/Code Info: All codes included
Quantity Affected: 60,109 cases
Reason for Recall
Does not declare the major food allergen "milk"
Distribution
Nationwide and Canada
Type: Voluntary: Firm initiated
Recall Initiated: 2023-07-07
Company
Cicero, IL
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 71 food recalls issued in the same week, part of 204 food-related FDA actions this month.
ZB Importing LLC has 8 FDA actions in our database, including 8 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 (ZB Importing LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does ZB Importing LLC have FDA actions?
ZB Importing LLC has 8 FDA actions in our database, including 8 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1305-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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