Life Raft TREATS ICE CREAM NOT FRIED CHICKEN Hand Crafted in Charleston S.C
Reason South Carolina Department of Health discovered the product contained Listeria monocytogenes.
Life Raft TREATS LIFE IS PEACHY recall
Recalled by Life Raft Treats Ice Cream Factory · North Charleston, SC, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
South Carolina Department of Health discovered the product contained 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
Life Raft TREATS LIFE IS PEACHY NET WT. 15 OZ BOX HAND CRAFTED IN CHARLESTON, SC
Quantity: 240/6ct box
Food: Fresh fruit
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 codes up to and including BEST BY 09042024.
Where it was sold
District of Columbia
FDA's distribution note: All fifty (50) states + DC
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as completed: 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
- Life Raft Treats Ice Cream Factory
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 5, 2023
- In FDA report of
- Oct 4, 2023
- FDA recall number
- F-1604-2023 · event 92993
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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