CLASS I Food recall · Reported 14 Jan 2026 · FDA Enforcement Report

Sam's Pecorino Romano grated recalled by Ambriola Co., Inc., The

Ambriola Co., Inc., The is recalling Sam's Pecorino Romano grated, distributed in 20 states. The recall was initiated on 21 Nov 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot number(s): 1000570107 1000570766 1000572513
Quantity recalled1,015 Bags (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
H-0371-2026
FDA event ID
98053
Recalling firm
Ambriola Co., Inc., The, West Caldwell, NJ
Classification
Class I
Status
Completed
Recall initiated
21 Nov 2025
FDA classified
6 Jan 2026
Reported
14 Jan 2026
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Listeria
Product category
Other

Timeline

21 Nov 2025Recall initiated by company
6 Jan 2026Classified by FDA+46 days
14 Jan 2026Published 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 tested positive for Listeria Monocytogenes.

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

Sam's Pecorino Romano grated, 1.5 lb Plastic Bags, 12 units per case

Where it was distributed

The recalled product was distributed to the following states: AZ, CA, CO, CT, DE, FL, GA, IL, IN, MA, ME, NJ, NY, OH, OR, PA, TX, VA, WA, WI

ArizonaCaliforniaColoradoConnecticutDelawareFloridaGeorgiaIllinoisIndianaMassachusettsMaineNew JerseyNew YorkOhioOregonPennsylvaniaTexasVirginiaWashingtonWisconsin

Questions about this recall

Why was it recalled?

Product tested positive for Listeria Monocytogenes.

Which lots are affected?

Lot number(s): 1000570107 1000570766 1000572513

Where was it sold?

The recalled product was distributed to the following states: AZ, CA, CO, CT, DE, FL, GA, IL, IN, MA, ME, NJ, NY, OH, OR, PA, TX, VA, WA, WI

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 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

7 other products · FDA event 98053

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