Food Recall Check
Class II · Moderate risk Terminated Initiated Feb 17, 2014 (13 years ago)

Cheese Pre-mix CF 21-1 recall

Recalled by Custom Ingredients LLC · New Braunfels, TX, United States

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

Why it was recalled

Undeclared wheat

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

Cheese Pre-mix, CF 21-1, in 50 lbs bags, intended to be used in the manufacture of cheese dip

Quantity: 10,300 Lbs (203-50 lbs. bags)

Food: Cheese Sauces, dips & dressings

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 # 090313-103, Exp date 3/3/2014; Exp date Lot #091 91 3-1 04, Exp date 3/19/2014; Lot # 093013-105, Exp date 3/30/2014; Lot # 102813-101, Exp date 4/28/2014; Lot # 112113-107, Exp date 5/21/2014; Lot# 121013-102, Exp date 6/10/2014; Lot # 012814-102, Exp date 7/28/2014

Where it was sold

New York Texas

FDA's distribution note: TX, NY

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
Custom Ingredients LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 17, 2014
In FDA report of
Sep 3, 2014
Terminated
Dec 11, 2014
FDA recall number
F-2350-2014 · event 67555
Official record
FDA enforcement report search

Also recalled with it (19 more products)

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

Showing 12 of 19.