The Recall Desk
Agency classClass IOur severity:CriticalFDA (Food)·H-0370-2026·Announced 2026-01-14

Boar's Head grated pecorino romano cups recalled after testing positive for Listeria

Ambriola is recalling 2,106 units of Boar's Head Grated Pecorino Romano in 6 oz cups after the product tested positive for Listeria monocytogenes.

The agency’s classification

FDA (Food): Class I

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

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 5/5 (Critical).

Highest-severity recall. The hazard can cause serious injury or death. Stop using the product now and follow the agency's instructions.

Our severity reasoning: Scored 5 because the FDA has classified this action as Class I, which the rubric maps directly to Critical.

Plain-English summary

Boar's Head Grated Pecorino Romano, 6 oz plastic cup and lid, 12 units per case, is being recalled by Ambriola Co., Inc.

The product tested positive for Listeria monocytogenes.

The recall covers 2,106 units from lot 1000572486. Distribution covered Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Illinois, Indiana, Massachusetts, Maine, New Jersey and other states. The FDA has classified the action as Class I, its most serious category.

Consumers who have a cup from this lot should not eat it and should follow the retailer's return instructions. Anyone who has eaten it and feels unwell should contact a healthcare provider.

The recalled product

Product
Boar's Head Grated Pecorino Romano, 6 oz Plastic Cup & Lid, 12 units per case
Affected units
2,106

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Lot number(s): 1000572486

Distribution

Part of a larger recall action

This product is one of 8 recalled by Ambriola Co., Inc., The under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 8 products in this recall →

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