Food Recall Check
Class I · High risk Terminated Initiated Mar 20, 2013 (14 years ago)

Heartland Gourmet Gluten Free rosemary basil pizza crust mix recall

Recalled by Heartland Gourmet, LLC · Lincoln, NE, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Some of the products contain milk but are labeled as dairy free.

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

Heartland Gourmet Gluten Free rosemary basil pizza crust mix, DAIRY FREE, packaged in 15.4-oz. boxes. Manufactured by: Heartland Gourmet, LLC, Lincoln, NE.

Quantity: 204/15.4-oz boxes

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.

Lot 073007 best buy date 09/2014

Where it was sold

Colorado Minnesota Texas

FDA's distribution note: The firm distributes their products to schools for fund raising events and also has internet distribution and some limited retail distribution. At this time we have records indicating distribution was made to TX, MN and CO. Distribution has been made to Canada.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. 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
Heartland Gourmet, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 20, 2013
In FDA report of
May 22, 2013
Terminated
Mar 19, 2014
FDA recall number
F-1386-2013 · event 64702
Official record
FDA enforcement report search

Also recalled with it (2 more products)

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