FDA recall record

Lakeview Farms, LLC Smilin' Bob's Key West Original Smoked Fish Dip 8oz plastic recall — FDA F-0093-2022

Undeclared Allergen - Egg

Class Iclassification
F-0093-2022official record ID
Nov 10, 2021report date

Recall record at a glance

Official recordF-0093-2022
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmLakeview Farms, LLC.
Report dateNov 10, 2021
Recall initiation dateOct 20, 2021
Quantity5532 containers (461 cases)
LocationDelphos, OH, United States

Official product description

Smilin' Bob's Key West Original Smoked Fish Dip 8oz plastic container with tamper proof lid 12 containers per case

Why the product was recalled

Undeclared Allergen - Egg

Distribution information

Product was distributed to the following states: GA and FL

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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