CLASS I Food recall · Reported 25 Jan 2023 · FDA Enforcement Report

Greco and Sons Dough Room Product No. 65 Garlic Knots 180/CS recalled

Sysco Merchandising and Supply is recalling Greco and Sons Dough Room Product No. 65 Garlic Knots 180/CS, distributed in Illinois, Maryland, Ohio, Pennsylvania, Virginia, West Virginia. The recall was initiated on 14 Dec 2022 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBest if Used By Date between 12/1/2022 and 06/01/2023
Quantity recalled25 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-0295-2023
FDA event ID
91334
Recalling firm
Sysco Merchandising and Supply, Houston, TX
Brand
Greco
Classification
Class I
Status
Terminated
Recall initiated
14 Dec 2022
FDA classified
19 Jan 2023
Reported
25 Jan 2023
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
Other

Timeline

14 Dec 2022Recall initiated by company
19 Jan 2023Classified by FDA+36 days
25 Jan 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

The dough ball products contain the undeclared allergen milk.

Product as listed by the FDA

Greco and Sons Dough Room Product No. 65 Garlic Knots 180/CS

Where it was distributed

OH, PA, VA, WV, IL, MD

IllinoisMarylandOhioPennsylvaniaVirginiaWest Virginia

Questions about this recall

Is Greco and Sons Dough Room Product No. 65 Garlic Knots 180/CS recalled?

Yes. Sysco Merchandising and Supply recalled Greco and Sons Dough Room Product No. 65 Garlic Knots 180/CS on 14 Dec 2022. The recall is Class I and its status is Terminated. Recall number F-0295-2023.

Why was it recalled?

The dough ball products contain the undeclared allergen milk.

Which lots are affected?

Best if Used By Date between 12/1/2022 and 06/01/2023

Where was it sold?

OH, PA, VA, WV, IL, MD

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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