FDA recall record

El Abuelito Cheese Quseo Fresco sold under the following brands and container recall — FDA F-0345-2021

Product may be contaminated with Listeria monocytogenes.

Class Iclassification
F-0345-2021official record ID
Mar 31, 2021report date

Recall record at a glance

Official recordF-0345-2021
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmEl Abuelito Cheese, Inc.
Report dateMar 31, 2021
Recall initiation dateFeb 17, 2021
QuantityN/A
LocationPaterson, NJ, United States

Official product description

Quseo Fresco sold under the following brands and container sizes - El Abuelito Cheese Brand - Queso Fresco Regular 12 oz.Plastic Container673130100003 Queso Fresco Promoci¿n 10 oz.Plastic Container673130100078 Queso Fresco de Hoja 12 oz.Plastic Container673130100065 Queso Fresco 5 Lb.Vacuum Packed673130100058 Queso Fresco Guatemala12 oz.Plastic Container673130100027 Rio Grande Food Products, Inc. Brand - Chirilagua Queso de Hacienda12 oz.Plastic Container738529005571 Queso Fresco Campestre con Hoja14 oz.Plastic Container812324031161 Queso Fresco Campestre Artesanal14 oz.Plastic Container738529002518 Queso Fresco con Hoja14 oz.Plastic Container738529004581 Queso Fresco Yorito12 oz.Plastic Container738529005564 Queso Fresco Olancho14 oz.Plastic Container812324031222 Cuajada Fresca Guatemalteca12 oz.Plastic Container738529001276 Cuajada Fresca Hondure¿a12 oz.Plastic Container738529001269 Cuajada Fresca Salvadore¿a 12 oz.Plastic Container738529001252 Rio Lindo Brand - Queso Fresco Mexicano 12 oz. Plastic Container 718122088587; Queso Fresco Hondure¿o 12 oz. Plastic Container 718122088591; Queso Fresco Salvadore¿o 12 oz. Plastic Container 718122088607

Why the product was recalled

Product may be contaminated with Listeria monocytogenes.

Distribution information

The product has been distributed in the following States: PA, NY, NJ, CT,DE, MA

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.

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