FDA recall record

Indalco Foods ***Dulce De Leche "Del Campo"***Ice Cream "Base" recall — FDA F-2391-2012

On June 28, 2011, Indalco Foods, Corp., Miami, FL initiated a voluntary recall of their product caramel milk spread ice cream base (dulce de leche…

Class Iclassification
F-2391-2012official record ID
Oct 3, 2012report date

Recall record at a glance

Official recordF-2391-2012
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmIndalco Foods Corp.
Report dateOct 3, 2012
Recall initiation dateJun 28, 2011
Quantity23/ 55 lbs. pails
LocationMiami, FL, United States

Official product description

***Dulce De Leche "Del Campo"***Ice Cream "Base" (Flavor)***FB 23546***Mfg. Date***Keep Refrigerated at 40*f***Lot#***Net Wt 55 LBS***Indalco Food Corp., Miami, FLA (305) 620 1444*** Caramel milk spread is packed in white plastic pails of 55 lbs. under the firm's brand name "Del Campo".

Why the product was recalled

On June 28, 2011, Indalco Foods, Corp., Miami, FL initiated a voluntary recall of their product caramel milk spread ice cream base (dulce de leche heladero). Product labeling does not list Milk.

Distribution information

US

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.