FDA recall record

LOVE CORN USA Sea Salt , Net WT recall — FDA F-1987-2018

Love Corn Inc. is Initiating a voluntary recall for 1,404 cases of its 1.6 oz. Sea Salt Love Corn product, due to the presence of low levels of undeclared…

Class IIclassification
F-1987-2018official record ID
Oct 3, 2018report date

Recall record at a glance

Official recordF-1987-2018
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmLOVE CORN USA
Report dateOct 3, 2018
Recall initiation dateSep 11, 2018
Quantity1,404 Cases
LocationHo Ho Kus, NJ, United States

Official product description

Love Corn, Sea Salt , Net WT. 1.6 Oz. Bags of 10 per cases

Why the product was recalled

Love Corn Inc. is Initiating a voluntary recall for 1,404 cases of its 1.6 oz. Sea Salt Love Corn product, due to the presence of low levels of undeclared peanuts.

Distribution information

Hudson Valley, NY Denver, CO

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

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.