Food Recall Check
Class II · Moderate risk Terminated Initiated Jan 16, 2015 (12 years ago)

The product label reads in part "***Buena Mexi Chicken Chowder *** Rill Foods*** recall

Recalled by Rill Foods · Thorp, WA, United States

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

Why it was recalled

Rill Foods distributed dry soup/chili mix products manufactured with cumin which was recalled due to the potential to be contaminated with peanut protein.

See the recall's own reason text for the specifics. All other reasons recalls.

What was recalled

The product label reads in part "***Buena Mexi Chicken Chowder *** Rill Foods***NET WT. 6.7 OZ.***" or "*** NET WT. 3.35 OZ.***"The product is packaged in a clear flexible laminate bag with a green card stock topper label which has white print. Case label is a white sticker and reads in part "Buena Chicken Chowder ***Rills Specialty Foods [email protected] 509-964-2520*** Production date is stamped on this label. Preparation directions are on the label. Small - 3.35 oz per package Large - 6.7 oz per package

Quantity: 357 units of the large size and 47 units of the small size

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.

The lot code is represented by DDMMYY and is located on the case label only. Lot Code - 102314

Where it was sold

Alaska California Colorado Idaho Kentucky Michigan Montana Oregon Washington

FDA's distribution note: Washington, Oregon, Montana, Idaho, Alaska, California, Michigan, Kentucky and Colorado.

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. 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
Rill Foods
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 16, 2015
In FDA report of
Mar 25, 2015
Terminated
Mar 17, 2015
FDA recall number
F-1432-2015 · event 70293
Official record
FDA enforcement report search

Also recalled with it (4 more products)

FDA files each product of one recall action separately; these share the same FDA event.