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CriticalFDAfda-F-1604-2023LISTERIA

Life Raft TREATS LIFE IS PEACHY NET WT. 15 OZ BOX HAND CRAFTED IN CHARLESTON, SC

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (listeria). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Category
Units Affected
240
Recall Date
September 5, 2023
Issuing Agency
Hazard
Listeria

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1604-2023.

South Carolina Department of Health discovered the product contained Listeria monocytogenes.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1604-2023.

Recall ongoing. Follow firm instructions.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Life Raft Treats Ice Cream Factory or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1604-2023.

Life Raft Treats Ice Cream Factory

FDA

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The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

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📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

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Life Raft Treats Ice Cream Factory Recall FAQ

Life Raft Treats Ice Cream Factory is the subject of a food safety report: Life Raft TREATS LIFE IS PEACHY NET WT. 15 OZ BOX HAND CRAFTED IN CHARLESTON, SC. The notice was published on September 5, 2023 by the U.S. Food and Drug Administration (FDA). Approximately 240 units are potentially affected.