ZB Importing LLC Recall: Milk not listed in Contains statement

🇺🇸 United States

1. February 15, 2025 - Recall initiated
2. March 19, 2025 - Reported by source
3. March 26, 2025 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0632-2025

Event ID

96337

Status

Terminated

Classification

Class II

Company

ZB Importing LLC

Product description

Ulker Dankek Roll Cake Strawberry , item 8298, 8.3oz foil pack, 8 per case, UPC 8690504066828

Quantity

145 cases

Reason

Milk not listed in Contains statement

Recall initiation date

February 15, 2025

Report date

March 19, 2025

Classification date

Not published in this source record

Termination date

March 26, 2025

Distribution pattern

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.

UPC, lot, and code information

UPC 8690504066828; L09 EXP 04/2025, L11 EXP 05/2025 and L07 EXP 07/2025

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Letter

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 96337 with 5 other product entries in Public Health Trace.

Responsible company: ZB Importing LLC

Other recalls from ZB Importing LLC

A map highlighting the states named in the source's distribution description.

Distributed No data published

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map

State	Distributed
Alabama	1
Arkansas	1
California	1
Connecticut	1
Colorado	1
District of Columbia	1
Delaware	1
Florida	1
Georgia	1
Illinois	1
Indiana	1
Kentucky	1
Louisiana	1
Massachusetts	1
Maryland	1
Michigan	1
Minnesota	1
Missouri	1
Mississippi	1
Nebraska	1
North Carolina	1
New Hampshire	1
New Jersey	1
New Mexico	1
New York	1
Ohio	1
Oklahoma	1
Pennsylvania	1
Rhode Island	1
South Carolina	1
Tennessee	1
Texas	1
Virginia	1
Washington	1
Wisconsin	1
West Virginia	1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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