Lavoi Corporation d/b/a/ Epi De France Fire House Subs Recall

Why it was recalled

Undeclared allergen: Bread products were manufactured using raw material (wheat gluten) that was recalled due to undeclared peanut and/or tree nut residue.

Product description

Fire House Subs, Medium White Sub Roll, and Large White Sub Roll, 48 and 45 count case, Lavoi Corporation, EPI Breads, 4710 West Ledbetter, Dallas, TX 75236.

Lot numbers, UPCs & expiration codes

Reference no. 10911 and 10912.

Where it was sold

AL, AR, AZ, CA, CO, FL, GA, IL, IN, KS, LA, MN, MO, MS, NC, NE, NY, PA, OH, OK, OR, SC, TX, VA, TN UT, and WA.

What to do if you have this product

Compare the brand, size, and lot/UPC codes on your package with the codes above.
If it matches, don't eat it. Return it to the store for a refund or throw it away.
Wash surfaces and containers that touched the product.
If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number: F-2757-2015
Classification: Class II
Status: Terminated
Recall initiated: Feb 24, 2015
FDA report date: Jul 1, 2015
Recall type: Voluntary: Firm initiated
Recalling firm: Lavoi Corporation d/b/a/ Epi De France

Original FDA data

Every field from FDA enforcement report F-2757-2015, exactly as published.

Show all FDA fields

City: Atlanta
State: GA
Status: Terminated
Country: United States
Event ID: 70581
Address: 1757 Tullie Cir Ne
Code information: Reference no. 10911 and 10912.
Postal code: 30329-2305
Report date: Jul 1, 2015
Product type: Food
Recall number: F-2757-2015
Classification: Class II
Recalling firm: Lavoi Corporation d/b/a/ Epi De France
Termination date: Jul 6, 2017
Reason for recall: Undeclared allergen: Bread products were manufactured using raw material (wheat gluten) that was recalled due to undeclared peanut and/or tree nut residue.
Voluntary / mandated: Voluntary: Firm initiated
Product description: Fire House Subs, Medium White Sub Roll, and Large White Sub Roll, 48 and 45 count case, Lavoi Corporation, EPI Breads, 4710 West Ledbetter, Dallas, TX 75236.
Distribution pattern: AL, AR, AZ, CA, CO, FL, GA, IL, IN, KS, LA, MN, MO, MS, NC, NE, NY, PA, OH, OK, OR, SC, TX, VA, TN UT, and WA.
Recall initiation date: Feb 24, 2015
Initial firm notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date: Jun 22, 2015

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-2757-2015, published Jul 1, 2015. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 2, 2026. Content last changed: Oct 2, 2026.

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