CLASS I Food recall · Reported 17 Dec 2025 · FDA Enforcement Report

Cacio e Pepe Arancini recalled by Stuffed Foods

Stuffed Foods is recalling Cacio e Pepe Arancini, distributed in Connecticut, Florida, Massachusetts, Missouri. The recall was initiated on 12 Nov 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesMFG ITEM #: 07312 LOT NUMBERS: 25114 produced on 4/25/2025
Quantity recalled51 cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0246-2026
FDA event ID
98010
Recalling firm
Stuffed Foods, Wilmington, MA
Brand
Stuffed
Classification
Class I
Status
Terminated
Recall initiated
12 Nov 2025
FDA classified
9 Dec 2025
Reported
17 Dec 2025
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Soy
Product category
Other

Timeline

12 Nov 2025Recall initiated by company
9 Dec 2025Classified by FDA+27 days
17 Dec 2025Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared Soy Protein Concentrate

Product as listed by the FDA

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

Where it was distributed

CT, MA, FL, MO

ConnecticutFloridaMassachusettsMissouri

Questions about this recall

Why was it recalled?

Undeclared Soy Protein Concentrate

Which lots are affected?

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

Where was it sold?

CT, MA, FL, MO

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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