Soft Serve on the Go brand Caramel Vanilla flavor; 8 fl oz; UPC 0-91404-15131-3
Summary
The FDA issued a Class I for Soft Serve on the Go brand Caramel Vanilla flavor; 8 fl oz; UPC 0-91404-15131-3 by Real Kosher Ice Cream, Inc.. Reason: Product may be contaminated with Listeria monocytogenes..
Details
Source
Food Recall
External ID
F-1479-2023
Action Date
2023-08-30
Status
Terminated
Category
food
Product Description
Soft Serve on the Go brand Caramel Vanilla flavor; 8 fl oz; UPC 0-91404-15131-3
Lot/Code Info: No Codes.
Quantity Affected: 54,076 Cases (12 cups per case) total all products
Reason for Recall
Product may be contaminated with Listeria monocytogenes.
Distribution
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
Type: Voluntary: Firm initiated
Recall Initiated: 2023-08-08
Company
Brooklyn, NY
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 63 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Real Kosher Ice Cream, Inc. has 5 FDA actions in our database, including 5 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (Real Kosher Ice Cream, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Real Kosher Ice Cream, Inc. have FDA actions?
Real Kosher Ice Cream, Inc. has 5 FDA actions in our database, including 5 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1479-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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