Jeni's Ice Cream Sandwich Chocolate Silk Pie Ice Cream 3.5 fl oz UPC 858241006882. Individually wrapped in plastic and p
Summary
The FDA issued a Class II for Jeni's Ice Cream Sandwich Chocolate Silk Pie Ice Cream 3.5 fl oz UPC 85824100688 by Totally Cool, Inc.. Reason: Possible contamination with Listeria monocytogenes.
Details
Source
Food Recall
External ID
F-1560-2024
Action Date
2024-08-07
Status
Terminated
Category
food
Product Description
Jeni's Ice Cream Sandwich Chocolate Silk Pie Ice Cream 3.5 fl oz UPC 858241006882. Individually wrapped in plastic and packaged in cardboard box, 3 sandwiches per box. 8 boxes per case.
Lot/Code Info: All Best by Dates: 07/24/25 to 05/23/2026 All Codes Between: 23205 to 24144 Plant Code: 2465
Quantity Affected: 12205 cases
Reason for Recall
Possible contamination with Listeria monocytogenes
Distribution
Distributed nationwide.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-06-13
Company
Owings Mills, MD
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 105 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Totally Cool, Inc. has 68 FDA actions in our database, including 68 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Totally Cool, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Totally Cool, Inc. have FDA actions?
Totally Cool, Inc. has 68 FDA actions in our database, including 68 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1560-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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