ICE CREAM HOUSE recalls Premium Sunday Quart Caramel Fudge (UPC 0-91404-153:40-9) due to potential Listeria monocytogenes contamination. Consumers should avoid consumption of affected products.
Products may be contaminated with Listeria monocytogenes.
ICE CREAM HOUSE is recalling Premium Sunday Quart Caramel Fudge because it may be contaminated with Listeria monocytogenes, a bacteria that can cause serious illness. This recall affects products sold with the specific UPC code listed.
Listeria monocytogenes is a bacteria that can cause food poisoning, leading to symptoms like fever, muscle aches, and in severe cases, miscarriage or meningitis. This specific product may have been contaminated during manufacturing or handling.
Consumers who purchased the Premium Sunday Quart Caramel Fudge with UPC 0-91404-15340-9 are affected. Those with weakened immune systems are at higher risk for serious illness from Listeria.
Check for the UPC code 0-91404-15340-9 on the product label. The product is labeled as 'Premium Sunday Quart / Caramel Fudge; Dairy / parve; 1 PACK'.
Look for the UPC code 0-91404-15340-9 on the product label to confirm if it is affected.
The recall record states that the product may be contaminated with Listeria monocytogenes, so it is not safe to consume.
The recall record does not specify a remedy, so consumers should avoid consuming the product and check the UPC code to confirm if it is affected.
Check for the UPC code 0-91404-15340-9 on the product label. The product is labeled as 'Premium Sunday Quart / Caramel Fudge; Dairy / parve; 1 PACK'.
We’ve drafted a message you can send ICE CREAM HOUSE to request your refund or repair — edit it as you like.
Subject: Recall F-1698-2023 — ICE CREAM HOUSE ICE CREAM HOUSE Hello, I own a ICE CREAM HOUSE that is covered by recall F-1698-2023 from ICE CREAM HOUSE. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
