RecallRadar
FDA · FoodClass I

Stuffed Foods LLC food recall: Stuffed Foods brand Cacio e Pepe Arancini

Undeclared allergens

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Terminated
Event ID
98010
Recall initiated
Nov 12, 2025
Classified by FDA
Dec 9, 2025
Posted in Enforcement Report
Dec 17, 2025
Terminated
Feb 11, 2026
Recalling firm
Stuffed Foods LLC
Firm location
Wilmington, MA, 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

Undeclared Soy Protein Concentrate

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 12, 2025. FDA classified it 27 days later, on Dec 9, 2025. Distribution reported by FDA: CT, MA, FL, MO Stuffed Foods LLC has 3 recalls in our records.

Recalled products (1)

  • H-0246-2026 Class I Terminated

    Stuffed Foods brand Cacio e Pepe Arancini; KEEP FROZEN; For institutional use only; Ready-to-cook; Cook to internal temp. of 165oF; Case pack: 3/3 lbs; Net Weight: 9lbs; UPC 00819985020787

    Codes / lots: MFG ITEM #: 07312 LOT NUMBERS: 25114 produced on 4/25/2025

    Quantity: 51 cases

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 98010
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.