FDA recall record

Industrias Alimenticias Kern's y Cia. S.C.A Ducal Brand Prepared Sauce Queso/Cheese, UPC recall — FDA F-2193-2014

Lab analysis detected the pH to be greater than 4.4

Class IIclassification
F-2193-2014official record ID
Jul 23, 2014report date

Recall record at a glance

Official recordF-2193-2014
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmIndustrias Alimenticias Kern's y Cia. S.C.A.
Report dateJul 23, 2014
Recall initiation dateAug 20, 2013
Quantity84 cases distributed from Goya Foods of Texas
LocationGuatemala, N/A, Guatemala

Official product description

Ducal Brand Prepared Sauce Queso/Cheese, UPC 088313-08328-6, Net Wt 4 oz, Product of Guatemala, C.A. Central American product made with quality by: Industrias Alimenticias Kern's Y/Cia, S.C.A., Km. 6 1/2 Carretera al Atlantico. Reg. D.G.R.V.C.S.D.R.C.A. B 658 The product was shipped in cases each of which included 4 paperboard cartons. Each paper board carton held 12-4 oz pouches.

Why the product was recalled

Lab analysis detected the pH to be greater than 4.4

Distribution information

Distribution was retail outlets in TX, OK, LA, CO, and TN

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: Letter.

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.