Food Recall Check
Class II · Moderate risk Terminated Initiated Jun 13, 2024 (2 years ago)

Marco Sweets & Spices Vanilla Chai Ice Cream Sandwiches recall

Recalled by Totally Cool, Inc. · Owings Mills, MD, United States

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

Why it was recalled

Possible contamination 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

Marco Sweets & Spices Vanilla Chai Ice Cream Sandwiches 3.8 fl oz UPC 860010682739. Individually wrapped in plastic. 3 sandwiches packaged in cardboard box, 8 boxes per case.

Quantity: 885 cases

Food: Ice cream Spices & seasonings Salads, sandwiches & prepared foods

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 Best by Dates Between: 11/28/25 to 11/29/25 Codes Between: 2405149 to 2405150 Plant Code: 2465

Where it was sold

Nationwide.

FDA's distribution note: Distributed nationwide.

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. 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
Totally Cool, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 13, 2024
In FDA report of
Aug 7, 2024
Terminated
Oct 8, 2024
FDA recall number
F-1558-2024 · event 94829
Official record
FDA enforcement report search

Also recalled with it (67 more products)

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

Showing 12 of 67.