FDA recall record

Lipari Foods Operating Company, LLC Backroad Country Spicy Cajun Mix 9 oz recall — FDA F-0199-2021

Undeclared Allergens: Milk

Class Iclassification
F-0199-2021official record ID
Jan 13, 2021report date

Recall record at a glance

Official recordF-0199-2021
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmLipari Foods Operating Company, LLC.
Report dateJan 13, 2021
Recall initiation dateDec 24, 2020
Quantity87 cases (1,044 - 9 oz.plastic bags)
LocationWarren, MI, United States

Official product description

Backroad Country Spicy Cajun Mix 9 oz (255g) plastic bag. Packed by Troyer Manufacturing Millersburg, OH 44654.

Why the product was recalled

Undeclared Allergens: Milk

Distribution information

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

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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