Ambriola Co., Inc., The recalls Sam's Pecorino Romano grated
Ambriola Co., Inc., The started this recall on November 21, 2025. The FDA classified it as Class I, the most serious category: there is a reasonable chance that eating the product could cause serious health problems or death. The reason given is listeria. It was distributed in 20 states. This recall is no longer considered active, but recalled products can stay in pantries and freezers for months.
- Status
- Closed / older
- Recall started
- November 21, 2025
- Company
- Ambriola Co., Inc., The
- Classification
- Class I (serious health risk)
- Where sold
- Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Illinois, Indiana, Massachusetts, Maine, New Jersey, New York, Ohio, Oregon, Pennsylvania, Texas, Virginia, Washington, Wisconsin
- Quantity
- 1,015 Bags (Units); 405 Bags (Units); 45 Bags (Units); 179 Bags (Units); 6,632 Units; 2,106 Units; 964 Bags (Units); 184 Units
Reason for recall (official wording)
Product tested positive for Listeria Monocytogenes.
Recalled products (official wording)
- Sam's Pecorino Romano grated, 1.5 lb Plastic Bags, 12 units per case
- Boar's Head Pecorino Romano Grated, 5-pound plastic bag (unit)
- Pinna Grated Pecorino Romano 2/10, 10-pound plastic bags (units)
- Ambriola Piccante grated Pecorino Romano, 5 and 10-pound plastic bags (units)
- Locatelli Grated Pecorino Romano 4 oz and 8 oz plastic cup & lid, 12 units per case
- Boar's Head Grated Pecorino Romano, 6 oz Plastic Cup & Lid, 12 units per case
- Locatelli Grated Pecorino Romano, 5 and 10-pound plastic bags (units)
- Locatelli Grated Pecorino Romano 48/8oz Shipper, Plastic Cup & Lid, 48 units per case
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
What to do
Compare the brand, size, lot code and dates on your package with the details above. If they match, do not eat it. Throw it away or return it to the store. Contact a healthcare provider if you feel unwell. Step-by-step guide.
Source: FDA Enforcement Report (openFDA), event 98053.