Food Recall Check
Class I · High risk Terminated Initiated Aug 8, 2023 (3 years ago)

Soft Serve on the Go brand Caramel Vanilla flavor recall

Recalled by Real Kosher Ice Cream, Inc. · Brooklyn, NY, United States

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

Why it was recalled

Product may be contaminated with Listeria monocytogenes.

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

Soft Serve on the Go brand Caramel Vanilla flavor; 8 fl oz; UPC 0-91404-15131-3

Quantity: 54,076 Cases (12 cups per case) total all products

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.

No Codes.

Where it was sold

California Colorado Connecticut District of Columbia Delaware Florida Illinois Massachusetts Maryland Michigan Minnesota North Carolina New Hampshire New Jersey New York Ohio Oregon Pennsylvania Virginia West Virginia

FDA's distribution note: CA, CO, CT, DC, DE, FL, IL, MA, MD, MI, MN, NC, NH, NJ, NY, OH, OR, PA, VA, WV; Mexico, United Kingdom, Canada, Belgium, and Brazil

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
Real Kosher Ice Cream, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Aug 8, 2023
In FDA report of
Aug 30, 2023
Terminated
Jun 14, 2024
FDA recall number
F-1479-2023 · event 92840
Official record
FDA enforcement report search

Also recalled with it (4 more products)

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