CLASS II Food recall · Reported 30 Dec 2020 · FDA Enforcement Report

Provolini Antipasta recalled by George DeLallo Co. Inc. New

George DeLallo Co. Inc. New Stanton Warehouse and Production is recalling Provolini Antipasta, distributed in Florida, Georgia. The recall was initiated on 24 Nov 2020 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot: W34310, Best By 04.APR.2021 (04 APR/ 2021)
Quantity recalled166 cases (12 units per 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-0184-2021
FDA event ID
86881
Classification
Class II
Status
Terminated
Recall initiated
24 Nov 2020
FDA classified
22 Dec 2020
Reported
30 Dec 2020
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Milk
Product category
Pasta & Noodles

Timeline

24 Nov 2020Recall initiated by company
22 Dec 2020Classified by FDA+28 days
30 Dec 2020Published 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

Product mis-packaging which lead to undeclared milk

Product as listed by the FDA

Provolini Antipasta Net Wt. 7 oz (198g) UPC 0-72368-39343-8

Where it was distributed

Distributed to warehouses in FL and GA

FloridaGeorgia

Questions about this recall

Why was it recalled?

Product mis-packaging which lead to undeclared milk

Which lots are affected?

Lot: W34310, Best By 04.APR.2021 (04 APR/ 2021)

Where was it sold?

Distributed to warehouses in FL and GA

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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