CLASS II Food recall · Reported 22 Feb 2023 · FDA Enforcement Report

Vietnamese Coffee Cheesecake Coconut Butter Biscuit Crust recalled

Amlag & Quibuyen is recalling Vietnamese Coffee Cheesecake Coconut Butter Biscuit Crust, distributed in Washington. The recall was initiated on 25 Jan 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesNo lot code. Expiration date 1/30/23.
Quantity recalled21/4 oz. units

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-0356-2023
FDA event ID
91622
Recalling firm
Amlag & Quibuyen, Seattle, WA
Classification
Class II
Status
Terminated
Recall initiated
25 Jan 2023
FDA classified
16 Feb 2023
Reported
22 Feb 2023
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Tree Nuts
Product category
Cakes & Pastries

Timeline

25 Jan 2023Recall initiated by company
16 Feb 2023Classified by FDA+22 days
22 Feb 2023Published 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

Vietnamese Coffee cheesecake is recalled because Coconut is declared in the ingredients statement, but Coconut is not declared in the Contains statement.

Product as listed by the FDA

Vietnamese Coffee Cheesecake Coconut Butter Biscuit Crust (4oz) - UPC 6 60845 37080 7.

Where it was distributed

Distributed in WA.

Washington

Questions about this recall

Why was it recalled?

Vietnamese Coffee cheesecake is recalled because Coconut is declared in the ingredients statement, but Coconut is not declared in the Contains statement.

Which lots are affected?

No lot code. Expiration date 1/30/23.

Where was it sold?

Distributed in WA.

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

3 other products · FDA event 91622

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