Locatelli Pecorino Romano Cheese Grated (Wegmans #270010) Packaged and sold by the pound Packaged in cylindrical clear p
Summary
The FDA issued a Class I for Locatelli Pecorino Romano Cheese Grated (Wegmans #270010) Packaged and sold by t by Wegmans Food Markets, Inc.. Reason: Product may be contaminated with Listeria monocytogenes..
Details
Source
Food Recall
External ID
H-0333-2026
Action Date
2025-12-31
Status
Terminated
Category
food
Product Description
Locatelli Pecorino Romano Cheese Grated (Wegmans #270010) Packaged and sold by the pound Packaged in cylindrical clear plastic tubs with lid UPC: 2-77580-XXXXX-7, where X is the unit price of the container
Lot/Code Info: Sell-by: 11/29/25 to Sell-by: 12/07/025
Quantity Affected: 2773.9 lbs.
Reason for Recall
Product may be contaminated with Listeria monocytogenes.
Distribution
NY, PA, MA, NJ, MD, VA, NC, DE, CT and DC
Type: Voluntary: Firm initiated
Recall Initiated: 2025-11-22
Company
Rochester, NY
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 33 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Wegmans Food Markets, Inc. has 28 FDA actions in our database, including 28 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 (Wegmans Food Markets, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Wegmans Food Markets, Inc. have FDA actions?
Wegmans Food Markets, Inc. has 28 FDA actions in our database, including 28 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0333-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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