FDA recall record

Ruiz Food Products El Monterey XXL Bean and Cheese Burrito recall — FDA F-2150-2019

Firm received two complaints of foreign object in frozen burrito product.

Class IIclassification
F-2150-2019official record ID
Sep 18, 2019report date

Recall record at a glance

Official recordF-2150-2019
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmRuiz Food Products Inc.
Report dateSep 18, 2019
Recall initiation dateAug 28, 2019
Quantity301 cases - 42 burritos per case
LocationDinuba, CA, United States

Official product description

El Monterey XXL Bean and Cheese Burrito; 9.5 oz. frozen burrito in film Microwaveable Case UPC: UPC 1 00 71007 06217 6; Sell unit UPC: 0 71007 06217 9

Why the product was recalled

Firm received two complaints of foreign object in frozen burrito product.

Distribution information

CT, MN, OR, SC

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.