Backroad Country Spicy Cajun Mix 9 oz (255g) plastic bag. Packed by Troyer Manufacturing…
Lipari Foods Operating Company, LLC. recalled this product and the FDA reported the enforcement action on 13 January 2021 as Class I. The recall was initiated by the firm. Undeclared Allergens: Milk
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
- Backroad Country Spicy Cajun Mix 9 oz (255g) plastic bag. Packed by Troyer Manufacturing Millersburg, OH 44654.
- Reason for recall
- Undeclared Allergens: Milk
- Recalling firm
- Lipari Foods Operating Company, LLC.
- Firm location
- Warren, Michigan, United States
- Classification
- Class I
- Status
- Terminated
- Recall number
- F-0199-2021
- Quantity
- 87 cases (1,044 - 9 oz.plastic bags)
- Distribution
- Product was distributed to the following states: Alabama Arkansas Colorado Georgia Illinois Indiana Kansas Maryland Michigan Missouri Mississippi Nebraska Ohio Oklahoma Pennsylvania South Carolina Tennessee Texas Virginia Wisconsin
- Initiated
- 24 December 2020
- Reported by FDA
- 13 January 2021
- Terminated
- 26 February 2021
- Firm notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product codes
- Lot Numbers: M24501, M26902, M28201 Product Numbers: Lipari 540896 Batch Numbers:Work Order s 839798, 840360
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class I means the FDA judged a reasonable probability that the product would cause serious health consequences or death. 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 record is the only one the FDA opened for its recall event, so it covers a single product code.
- The recall ran for 2 months, from 24 December 2020 to termination on 26 February 2021. 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 FDA published the enforcement report 3 weeks 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.
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: milk.
Other records from Lipari Foods Operating Company, LLC.
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 54 other records name this firm.
All 55 records for Lipari Foods Operating Company, LLC.
All 2021 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.