Boar's Head Grated Pecorino Romano, 6 oz Plastic Cup & Lid, 12 units per case
Summary
The FDA issued a Class I for Boar's Head Grated Pecorino Romano, 6 oz Plastic Cup & Lid, 12 units per case by Ambriola Co., Inc., The. Reason: Product tested positive for Listeria Monocytogenes..
Details
Source
Food Recall
External ID
H-0370-2026
Action Date
2026-01-14
Status
Completed
Category
food
Product Description
Boar's Head Grated Pecorino Romano, 6 oz Plastic Cup & Lid, 12 units per case
Lot/Code Info: Lot number(s): 1000572486
Quantity Affected: 2,106 Units
Reason for Recall
Product tested positive for Listeria Monocytogenes.
Distribution
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
Type: Voluntary: Firm initiated
Recall Initiated: 2025-11-21
Company
West Caldwell, NJ
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 36 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Ambriola Co., Inc., The has 8 FDA actions in our database, including 8 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Ambriola Co., Inc., The) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Ambriola Co., Inc., The have FDA actions?
Ambriola Co., Inc., The has 8 FDA actions in our database, including 8 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0370-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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