CLASS II Food recall · Reported 26 Feb 2020 · FDA Enforcement Report

Cheesecake with Poppy seeds in plastic clam shell recalled

Forest View Bakery is recalling Cheesecake with Poppy seeds in plastic clam shell, distributed in Illinois. The recall was initiated on 6 Feb 2020 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesSell by date-02/10/2020
Quantity recalled6 units and 5, 216oz sheet cakes for sale by the slice

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-0717-2020
FDA event ID
84901
Recalling firm
Forest View Bakery, Chicago, IL
Classification
Class II
Status
Terminated
Recall initiated
6 Feb 2020
FDA classified
19 Feb 2020
Reported
26 Feb 2020
Type
Voluntary: Firm initiated
Customers notified by
Visit
Reason category
Undeclared Milk
Product category
Cakes & Pastries

Timeline

6 Feb 2020Recall initiated by company
19 Feb 2020Classified by FDA+13 days
26 Feb 2020Published in enforcement report+7 days

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

Reason for recall

Undeclared allergens of milk, almonds, and wheat

Product as listed by the FDA

Forest View Bakery Cheesecake with Poppy seeds in 18oz plastic clam shell UPC 745454333860

Where it was distributed

Four retailers in Chicago IL

Illinois

Questions about this recall

Why was it recalled?

Undeclared allergens of milk, almonds, and wheat

Which lots are affected?

Sell by date-02/10/2020

Where was it sold?

Four retailers in Chicago IL

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

4 other products · FDA event 84901

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