Creative Snacks Co recall

Recalled by Creative Snacks Co., LLC · Greensboro, NC, United States

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

Why it was recalled

Potential presence of Listeria Monocytogenes

Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

Creative Snacks Co. Sunny Day Splendor, 10 lb. bulk, UPC 816512014653; Creative Snacks Co. Sunny Day Splendor 10 oz. cup, UPC 816512010983

Quantity: 90 cases

Food: Chips & snacks

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.

Creative Snacks 10 lb. bulk 1192031716; Creative Snacks 10 oz. cup 2930041916

Where it was sold

California Connecticut Delaware Georgia Indiana Massachusetts Maine Minnesota North Carolina New Jersey New York South Carolina Texas Utah

FDA's distribution note: CA, CT, DE, GA, IN, ME, MA, MN, NJ, NY, NC, SC, TX, UT

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: Creative Snacks Co., LLC
Initiated by: Voluntary: Firm initiated
Recall initiated: May 5, 2016
In FDA report of: Aug 10, 2016
Terminated: Jul 18, 2017
FDA recall number: F-1866-2016 · event 74063
Official record: FDA enforcement report search

Also recalled with it (6 more products)

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

Class I · High risk Terminated Listeria May 5, 2016