Baraka Gourmet Pastry Kunafe 6.7oz., UPC 822514291060, 18 retail units per wholesale case
Summary
The FDA issued a Class II for Baraka Gourmet Pastry Kunafe 6.7oz., UPC 822514291060, 18 retail units per whole by ZIYAD BROTHERS IMPORTING. Reason: May contain partially hydrogenated oils.
Details
Source
Food Recall
External ID
H-0378-2026
Action Date
2026-01-14
Status
Terminated
Category
food
Product Description
Baraka Gourmet Pastry Kunafe 6.7oz., UPC 822514291060, 18 retail units per wholesale case
Lot/Code Info: LOT 164024 EXP 15.JUN.2026 LOT 340024 EXP 07.DEC.2025 LOT 049025 EXP 18.FEB.2027 LOT 155025 EXP 04.JUN.2027
Quantity Affected: 575 cases
Reason for Recall
May contain partially hydrogenated oils
Distribution
Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2025-12-17
Company
Bolingbrook, 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 36 food recalls issued in the same week, part of 204 food-related FDA actions this month.
ZIYAD BROTHERS IMPORTING 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 (ZIYAD BROTHERS IMPORTING) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does ZIYAD BROTHERS IMPORTING have FDA actions?
ZIYAD BROTHERS IMPORTING 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 "H-0378-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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