Food Recall Check
Class II · Moderate risk Terminated Initiated Nov 20, 2013 (13 years ago)

Lemon Butter Cookies sold under the Lambs Farm brand and packaged in a plastic bag with a recall

Recalled by The Lambs Farm, Inc. · Libertyville, IL, United States

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

Why it was recalled

The labels do not declare milk and wheat allergens.

Undeclared allergens: Milk 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

Lemon Butter Cookies sold under the Lambs Farm brand and packaged in a plastic bag with a net weight of 10 oz.

Quantity: 10 oz packages: 342 bags; 7 lbs bulk packages: 1 bag

Food: Milk & dairy 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.

All batches coded with dates 7/1/2013 through 11/14/2013.

Where it was sold

Nationwide.

Florida Illinois Indiana Minnesota Pennsylvania Wisconsin

FDA's distribution note: US: Nationwide (FL, IL, IN, MN, PA, WI)

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 milk, 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
The Lambs Farm, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Nov 20, 2013
In FDA report of
Feb 5, 2014
Terminated
Apr 11, 2016
FDA recall number
F-1431-2014 · event 66901
Official record
FDA enforcement report search

Also recalled with it (8 more products)

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