CLASS II Food recall · Reported 6 Mar 2024 · FDA Enforcement Report

Oggi Pizza Plant Based Americana Beyond Meat Crumbles recalled

Pasta Oggi is recalling Oggi Pizza Plant Based Americana Beyond Meat Crumbles on Cauliflower Crust, gluten-free, distributed in California, Illinois, Washington. The recall was initiated on 7 Feb 2024 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot: 23-200. Best Before: BB: 2024 JL 19
Quantity recalled5040 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-0934-2024
FDA event ID
94027
Recalling firm
Pasta Oggi, Saint-Leonard
Brand
Oggi
Classification
Class II
Status
Terminated
Recall initiated
7 Feb 2024
FDA classified
27 Feb 2024
Reported
6 Mar 2024
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Milk
Product category
Frozen Pizza

Timeline

7 Feb 2024Recall initiated by company
27 Feb 2024Classified by FDA+20 days
6 Mar 2024Published in enforcement report+8 days

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

Reason for recall

Undeclared milk

Product as listed by the FDA

Oggi Pizza Plant Based Americana Beyond Meat Crumbles on Cauliflower Crust, gluten-free frozen pizza - cook before serving, net wt. 13.76oz (390g). One pizza wrapped in plastic film in a cardboard box. Retail box UPC 6 28451 68487 9. There are 12 pizza per case, and each case has UPC 1062845 1684876.

Where it was distributed

Distributed in IL, CA and WA.

CaliforniaIllinoisWashington

Questions about this recall

Why was it recalled?

Undeclared milk

Which lots are affected?

Lot: 23-200. Best Before: BB: 2024 JL 19

Where was it sold?

Distributed in IL, CA and 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.

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