Chipwich Vanilla Chocolate Chip Ice Cream Sandwich 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

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

Chipwich Vanilla Chocolate Chip Ice Cream Sandwich 4 fl oz sold as 3-pack, 10-pack, and 24 (single serve) pack. Sandwiches individually wrapped in plastic. Product packaged in cardboard boxes. UPCs 810493034013, 810493035010, and 810493030022. 12 boxes/8 boxes/24 boxes per case.

Quantity: 113315 cases

Food: Ice cream Chocolate & candy 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 02/23/25 to 12/21/25 Club pack (10 units): Lot# 23298-24172 24 pack (Single Serve): Lot# 23298-24164 3 packs: Lot# 23298-24136

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-1569-2024 · 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.

Class I · High risk Terminated Listeria Jun 13, 2024