FDA recall record

La Terra Fina USA Chunky Spinach Artichoke and Parmesan Dip: Gluten Free, Trans recall — FDA F-1869-2013

One lot Spinach Artichoke & Parmesan dip contains the ingredient and nutrition information for Caramelized onion dip. Both dips have the same allergens…

Class IIIclassification
F-1869-2013official record ID
Sep 11, 2013report date

Recall record at a glance

Official recordF-1869-2013
CategoryFood Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmLa Terra Fina USA, Inc.
Report dateSep 11, 2013
Recall initiation dateAug 2, 2013
Quantity1130 cases (6/10 oz tubs per carton)
LocationUnion City, CA, United States

Official product description

Chunky Spinach Artichoke and Parmesan Dip: Gluten Free, Trans Fat Free. Net WT. 10 oz., (.625 lb,284g Made with real cream cheese. Plastic square tub La Terra Fina Union City, CA 94587

Why the product was recalled

One lot Spinach Artichoke & Parmesan dip contains the ingredient and nutrition information for Caramelized onion dip. Both dips have the same allergens statement - Milk, Soy and Egg.

Distribution information

CA, CO, TX, IN..

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

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.