Cinnamon Frozen Pops recall

Recalled by Seattle Pops · Seattle, WA, United States

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

Why it was recalled

Ice Cream Bars/Pops are recalled due to the potential to be contaminated with Listeria monocytogenes. These products contain an ice cream based ingredient that was manufactured and recalled by Snoqualmie Gourmet Ice Cream, Inc.

Pathogen: Listeria

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

Cinnamon Frozen Pops, 4.0 fl oz. frozen pop is individually packaged in a sealed plastic bag; 24 pops/case. Product is labeled in part, "***cream, milk, skim milk powder, non-gmo cane sugar, vanilla, cinnamon, less than 0.4% stabilizer (carob bean gum, guar gum, soy lecithin, carrageenan)***Seattle Pops PO Box 31285 Seattle, WA 98103***". No UPC code.

Quantity: 48 pops

Food: Spices & seasonings

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.

Product is not coded.

Where it was sold

Washington

FDA's distribution note: Product was distributed in Washington state.

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: Seattle Pops
Initiated by: Voluntary: Firm initiated
Recall initiated: Dec 23, 2014
In FDA report of: Apr 15, 2015
Terminated: Apr 14, 2015
FDA recall number: F-1886-2015 · event 70153
Official record: FDA enforcement report search