Ambriola Co., Inc., The
Complete recall history across all FDA and CPSC categories — 8 total recalls
Ambriola Co., Inc., The appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.
Food Recalls (8)
FDA food safety enforcement actions by Ambriola Co., Inc., The
| Date | Product | Reason | Class |
|---|---|---|---|
| Nov 21, 2025 | Locatelli Grated Pecorino Romano 48/8oz Shipper, Plastic Cup & Lid, 48 units ... | Product tested positive for Listeria Monocytogenes. | Class I |
| Nov 21, 2025 | Locatelli Grated Pecorino Romano, 5 and 10-pound plastic bags (units) | Product tested positive for Listeria Monocytogenes. | Class I |
| Nov 21, 2025 | Boar's Head Grated Pecorino Romano, 6 oz Plastic Cup & Lid, 12 units per case | Product tested positive for Listeria Monocytogenes. | Class I |
| Nov 21, 2025 | Locatelli Grated Pecorino Romano 4 oz and 8 oz plastic cup & lid, 12 units pe... | Product tested positive for Listeria Monocytogenes. | Class I |
| Nov 21, 2025 | Ambriola Piccante grated Pecorino Romano, 5 and 10-pound plastic bags (units) | Product tested positive for Listeria Monocytogenes. | Class I |
| Nov 21, 2025 | Pinna Grated Pecorino Romano 2/10, 10-pound plastic bags (units) | Product tested positive for Listeria Monocytogenes. | Class I |
| Nov 21, 2025 | Boar's Head Pecorino Romano Grated, 5-pound plastic bag (unit) | Product tested positive for Listeria Monocytogenes. | Class I |
| Nov 21, 2025 | Sam's Pecorino Romano grated, 1.5 lb Plastic Bags, 12 units per case | Product tested positive for Listeria Monocytogenes. | Class I |
Frequently Asked Questions
A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.
Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.
The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.
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