FDA recall record

Palmer and Company Sea Salt Caramel Hearts, Net Wt 12 OZ recall — FDA F-0751-2018

During packaging, the firm observed a peanut stuck to the outside of caramel heart. Peanuts are not declared on the label.

Class IIclassification
F-0751-2018official record ID
Feb 14, 2018report date

Recall record at a glance

Official recordF-0751-2018
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmPalmer and Company
Report dateFeb 14, 2018
Recall initiation dateJan 17, 2018
Quantity63 cases
LocationSioux City, IA, United States

Official product description

Sea Salt Caramel Hearts, Net Wt 12 OZ (340 g), Made by Palmer Candy Company, Sioux City, Iowa. UPC 77232-17091

Why the product was recalled

During packaging, the firm observed a peanut stuck to the outside of caramel heart. Peanuts are not declared on the label.

Distribution information

Product distributed to one distribution center which further distributed to retail stores in CO, IA, MN, NE, SD, and WY.

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: 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.

Related recall records

Other records from the same recalling company are shown first when available.