Epi breads, 7" Wheat Hoagie Wide, Net Weight 10.8 lbs, Lavoi Corporation, EPI Breads…
Lavoi Corporation d/b/a/ Epi De France recalled this product and the FDA reported the enforcement action on 1 July 2015 as Class II. The recall was initiated by the firm. Undeclared allergen: Bread products were manufactured using raw material (wheat gluten) that was recalled due to undeclared peanut and/or tree nut residue.
The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- Epi breads, 7" Wheat Hoagie Wide, Net Weight 10.8 lbs, Lavoi Corporation, EPI Breads, 4710 West Ledbetter, Dallas, TX 75236.
- 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.
- Recalling firm
- Lavoi Corporation d/b/a/ Epi De France
- Firm location
- Atlanta, Georgia, United States
- Classification
- Class II
- Status
- Terminated
- Recall number
- F-2754-2015
- Quantity
- Not stated
- Distribution
- 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.
- Initiated
- 24 February 2015
- Reported by FDA
- 1 July 2015
- Terminated
- 6 July 2017
- Firm notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product codes
- Reference no. 10849.
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This is one of 22 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 22 separate recalls, which almost every published figure does, overstates it by a factor of 22. Every product code in this event is listed together on the record that covers the whole recall, which is the page a search engine is pointed to for all 22 of them.
- The recall ran for 2.4 years, from 24 February 2015 to termination on 6 July 2017. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The distribution pattern names 25 states, and the FDA published the enforcement report 4 months after the firm began the recall.
- The product description on this record names no food this site can classify, so it appears on no food-type page. That is a limit of the description rather than of the recall.
Named in the distribution pattern: Alabama, Arkansas, Arizona, California, Colorado, Florida, Georgia, Illinois, Indiana, Kansas, Louisiana, Minnesota, Missouri, Mississippi, North Carolina, Nebraska, New York, Pennsylvania, Ohio, Oklahoma, Oregon, South Carolina, Texas, Virginia, Washington. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
What this recall was for
Undeclared allergens
An undeclared allergen recall means a food contained one of the major allergens and the label did not say so, either because the wrong label was applied or because an ingredient carried an allergen nobody traced.
A preventive controls plan covers an undeclared allergen under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.
- 21 CFR 117.135(c)(2)
- Food allergen controls: the written preventive controls that keep an allergen out of a food it does not belong in, and that get the allergens present onto the label.
- 21 CFR 101.4
- Ingredient declaration: every ingredient listed by its common name, in descending order of predominance, on the label of a packaged food.
- 21 CFR 117 subpart G
- Supply-chain programme: the approval and verification a receiving facility runs on a supplier when the hazard is controlled before the ingredient arrives.
The allergens named in this record: wheat, peanuts, tree nuts.
Other records from Lavoi Corporation d/b/a/ Epi De France
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 21 other records name this firm.
All 22 records for Lavoi Corporation d/b/a/ Epi De France
All 2015 recalls · All FDA food recall data
21 CFR 117.135(c)(2) is the clause behind this recall, and it is one somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.