Food Recall Check
Class II · Moderate risk Terminated Initiated Mar 19, 2013 (14 years ago)

Miravalle brand "Pan Rallado Sazonado" recall

Recalled by Miravalle Food, Inc · El Monte, CA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

In response to a FDA inspection, the firm initiated this recall due to undeclared wheat and no nutritional facts listed, for the product "Pan Rallado Sazonado".

Undeclared allergen: Wheat

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Miravalle brand "Pan Rallado Sazonado", 8 oz. Seasoned bread crumbs. Also packaged in 12 pack. Product labeling reads in part:"Miravalle PAN RALLADO SAZONADO SEASONED BREAD CRUMBS Net Wt. 8 Oz.***Packed and Distributed by: Miravalle El Monte, CA 91733***".

Quantity: 312 dz.

Food: Bread & bakery

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

UPC: 7 12810-00812 Lot numbers: 0010 Expiration date: 08/2013

Where it was sold

California Colorado Idaho Nevada Oregon Utah Washington

FDA's distribution note: US States: CA, NV, OR, ID, WA, UT, and CO.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to wheat; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Miravalle Food, Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 19, 2013
In FDA report of
Apr 3, 2013
Terminated
Sep 25, 2013
FDA recall number
F-1252-2013 · event 52857
Official record
FDA enforcement report search

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