Food Recall Check
Class II · Moderate risk Terminated Initiated Jan 14, 2015 (12 years ago)

Joe Paatis recall

Recalled by Gourmet Foods International · Atlanta, GA, United States

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

Why it was recalled

Products were manufactured with cumin found to contain undeclared peanuts.

Undeclared allergen: Peanut

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

Joe Paatis, CAJUN SEAFOOD SEASONING, 3.5oz., Joe Pattis.com 524 South B Street, Pensacola, FL 32501.

Quantity: N/A

Food: Spices & seasonings

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.

Item no. 25842, Exp. Dates between 2/21/15-12/28/16

Where it was sold

Alabama Arkansas Colorado Florida Georgia Indiana Kentucky Louisiana Michigan Missouri North Carolina New York Ohio South Carolina Tennessee Texas

FDA's distribution note: AL, AR, CO, FL, GA, IN, KY, LA, MI, MO, NC, NY, OH, SC, TN & TX.

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 peanut; 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
Gourmet Foods International
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 14, 2015
In FDA report of
Apr 22, 2015
Terminated
Feb 1, 2017
FDA recall number
F-1974-2015 · event 70316
Official record
FDA enforcement report search

Also recalled with it (32 more products)

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

Showing 12 of 32.