FDA recall record

JTM Provisions Co Bean & Cheese Burrito Filling, 10 lb bags Labeled in part recall — FDA F-1902-2013

Undeclared eggs in the product. The firm was notified by their customer that the product contains pasta. The pasta contains eggs which is not declared on…

Class Iclassification
F-1902-2013official record ID
Sep 25, 2013report date

Recall record at a glance

Official recordF-1902-2013
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmJTM Provisions Co Inc.
Report dateSep 25, 2013
Recall initiation dateSep 11, 2013
Quantity821 cases/3/10 lb bags
LocationHarrison, OH, United States

Official product description

Bean & Cheese Burrito Filling, 10 lb bags Labeled in part "13210 B 1 77220 13:38 KEEP FROZEN BEAN & CHEESE BURRITO FILLING***INGREDIENTS: COOKED PINTO BEANS, WATER, CHEDDAR CHEESE***SOYBEAN OIL***STARCH-MODIFIED, ONIONS, CHEESE SAUCE BASE***CONTAINS LESS THAN 2% OF CHILI PEPPER, SALT, CHICKEN BASE***SODIUM PHOSPHATES, SPICE, CARAMEL COLOR DEHYDRATED, GARLIC, ANNATTTO EXTRACT." CONTAINS: Soy, Milk, Wheat JTM Food Group 200 Sales Dr. Harrison, OH 45030 Phone 800.626.2308.

Why the product was recalled

Undeclared eggs in the product. The firm was notified by their customer that the product contains pasta. The pasta contains eggs which is not declared on the label.

Distribution information

Product was shipped to one manufacturer in MN.

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

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