CLASS I Food recall · Reported 19 Mar 2025 · FDA Enforcement Report

Ulker Biskrem Cocoa Biscuit recalled by ZB Importing

ZB Importing is recalling Ulker Biskrem Cocoa Biscuit, distributed in 36 states. The recall was initiated on 15 Feb 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesL07 EXP 06/2025 and L09 EXP 9/2025
Quantity recalled1881 Cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0633-2025
FDA event ID
96337
Recalling firm
ZB Importing, Cicero, IL
Classification
Class I
Status
Terminated
Recall initiated
15 Feb 2025
FDA classified
13 Mar 2025
Reported
19 Mar 2025
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Egg
Product category
Chocolate

Timeline

15 Feb 2025Recall initiated by company
13 Mar 2025Classified by FDA+26 days
19 Mar 2025Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared wheat and egg

Product as listed by the FDA

Ulker Biskrem Cocoa Biscuit, item 8836, 10.6oz foil pack, 8 per case, UPC 8690504114628

Where it was distributed

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.

AlabamaArkansasCaliforniaColoradoConnecticutDistrict of ColumbiaDelawareFloridaGeorgiaIllinoisIndianaKentuckyLouisianaMassachusettsMarylandMichiganMinnesotaMissouriMississippiNorth Carolina

Questions about this recall

Is Ulker Biskrem Cocoa Biscuit recalled?

Yes. ZB Importing recalled Ulker Biskrem Cocoa Biscuit on 15 Feb 2025. The recall is Class I and its status is Terminated. Recall number F-0633-2025.

Why was it recalled?

Undeclared wheat and egg

Which lots are affected?

L07 EXP 06/2025 and L09 EXP 9/2025

Where was it sold?

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.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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