Food Recall Check
Class I · High risk Terminated Initiated Mar 26, 2015 (12 years ago)

Silver Lake Easter Egg Cookies recall

Recalled by Silver Lake Cookie Co., Inc. · Islip, NY, United States

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

Why it was recalled

Silver Lake Cookie Co., Inc. recalls Easter Egg Cookie due to the presence of undeclared egg.

Undeclared allergen: Egg

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

Silver Lake Easter Egg Cookies, NET WT. 8 OZ (226g), UPC 0 37695 49817 1. Silver Lake Cookie Company, Inc. 141 Freeman Ave., Islip, NY 11751. MADE IN THE USA.

Quantity: 259 cases/24 pieces

Food: 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 lot numbers

Where it was sold

Connecticut Georgia Illinois Indiana Massachusetts Minnesota New Jersey New York Pennsylvania Wisconsin

FDA's distribution note: CT, GA, IN, IL, MA, MN, NJ, NY, PA & WI

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. The risk from an undeclared allergen is to people allergic to egg; 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
Silver Lake Cookie Co., Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 26, 2015
In FDA report of
Apr 29, 2015
Terminated
May 9, 2017
FDA recall number
F-2031-2015 · event 70855
Official record
FDA enforcement report search

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