Life Raft TREATS LIFE IS PEACHY NET WT. 15 OZ BOX HAND CRAFTED IN CHARLESTON, SC
Summary
The FDA issued a Class I for Life Raft TREATS LIFE IS PEACHY NET WT. 15 OZ BOX HAND CRAFTED IN CHARLESTON, S by Life Raft Treats Ice Cream Factory. Reason: South Carolina Department of Health discovered the product contained Listeria monocytogenes..
Details
Source
Food Recall
External ID
F-1604-2023
Action Date
2023-10-04
Status
Completed
Category
food
Product Description
Life Raft TREATS LIFE IS PEACHY NET WT. 15 OZ BOX HAND CRAFTED IN CHARLESTON, SC
Lot/Code Info: All codes up to and including BEST BY 09042024.
Quantity Affected: 240/6ct box
Reason for Recall
South Carolina Department of Health discovered the product contained Listeria monocytogenes.
Distribution
All fifty (50) states + DC
Type: Voluntary: Firm initiated
Recall Initiated: 2023-09-05
Company
North Charleston, SC
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 185 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Life Raft Treats Ice Cream Factory has 2 FDA actions in our database, including 2 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 (Life Raft Treats Ice Cream Factory) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Life Raft Treats Ice Cream Factory have FDA actions?
Life Raft Treats Ice Cream Factory has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1604-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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