Ambriola Co., Inc., The Recall: Product tested positive for Listeria Monocytogenes.

🇺🇸 United States

1. November 21, 2025 - Recall initiated
2. January 14, 2026 - Reported by source

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

H-0371-2026

Event ID

98053

Status

Completed

Classification

Class I

Company

Ambriola Co., Inc., The

Product description

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

Quantity

1,015 Bags (Units)

Reason

Product tested positive for Listeria Monocytogenes.

Recall initiation date

November 21, 2025

Report date

January 14, 2026

Classification date

Not published in this source record

Termination date

Not terminated as of this source record

Distribution pattern

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

UPC, lot, and code information

Lot number(s): 1000570107 1000570766 1000572513

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 98053 with 7 other product entries in Public Health Trace.

Responsible company: Ambriola Co., Inc., The

Other recalls from Ambriola Co., Inc., The

A map highlighting the states named in the source's distribution description.

Distributed No data published

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map

State	Distributed
Arizona	1
California	1
Colorado	1
Connecticut	1
Delaware	1
Florida	1
Georgia	1
Illinois	1
Indiana	1
Massachusetts	1
Maine	1
New Jersey	1
New York	1
Ohio	1
Oregon	1
Pennsylvania	1
Texas	1
Virginia	1
Washington	1
Wisconsin	1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Completed." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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