RecallRadar
FDA · FoodClass I

Wegmans Food Markets, Inc. food recall: Locatelli Pecorino Romano Cheese Grated

ListeriaMicrobial contamination

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Terminated
Event ID
98044
Recall initiated
Nov 22, 2025
Classified by FDA
Dec 19, 2025
Posted in Enforcement Report
Dec 31, 2025
Terminated
Feb 11, 2026
Recalling firm
Wegmans Food Markets, Inc.
Firm location
Rochester, NY, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Products in this event
1

What to do

Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.

View the official FDA record ↗

Reason for recall

Product may be contaminated with Listeria monocytogenes.

What the classification means

  • Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.

About this recall

The firm started this recall on Nov 22, 2025. FDA classified it 27 days later, on Dec 19, 2025. Distribution reported by FDA: NY, PA, MA, NJ, MD, VA, NC, DE, CT and DC Wegmans Food Markets, Inc. has 42 recalls in our records.

Recalled products (1)

  • H-0333-2026 Class I Terminated

    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

    Codes / lots: Sell-by: 11/29/25 to Sell-by: 12/07/025

    Quantity: 2773.9 lbs.

Source and freshness

Source
U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
Official notice
FDA Enforcement Report, event 98044
Raw record
openFDA API (JSON)
Dataset last updated by FDA
Nov 3, 2026
Imported by RecallRadar
Nov 4, 2026

Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.

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