Ulker Kekstra Mini strawberry, item 3792, 5.3oz foil pack, 10 per case, UPC 8690766082307
Summary
The FDA issued a Class II for Ulker Kekstra Mini strawberry, item 3792, 5.3oz foil pack, 10 per case, UPC 869 by ZB Importing LLC. Reason: Milk not declared as the major food allergen source for the ingredient Whey.
Details
Source
Food Recall
External ID
F-0630-2025
Action Date
2025-03-19
Status
Terminated
Category
food
Product Description
Ulker Kekstra Mini strawberry, item 3792, 5.3oz foil pack, 10 per case, UPC 8690766082307
Lot/Code Info: L07 04/2025 and L11 EXP 11/2025
Quantity Affected: 433 cases
Reason for Recall
Milk not declared as the major food allergen source for the ingredient Whey
Distribution
Products were distributed through retail stores in Ontario, Canada and the following US states AL, AR, CA, CT, CO, DC, DE, FL, GA, IL, IN, KY, LA, MA, MD, MI, MN, MO, MS, NE, NC, NH, NJ, NM, NY, OH, OK, PA, RI, SC, TN, TX, VA, WA, WI and WV.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-02-15
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 55 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-0630-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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