ICE CREAM HOUSE recalls Premium Sorbet Quart, Trio, and Vanilla Strawberry Mango products due to potential Listeria monocytogenes contamination. Consumers should check UPC 0-91404-1:15162-7 for affected items.
Products may be contaminated with Listeria monocytogenes.
ICE CREAM HOUSE is recalling Premium Sorbet Quart, Trio, and Vanilla Strawberry Mango products because they may be contaminated with Listeria monocytogenes. This bacteria can cause serious illness, especially for pregnant women, newborns, and those with weakened immune systems.
Listeria monocytogenes is a bacteria that can cause serious infections in vulnerable groups. It spreads through contaminated food and can lead to miscarriages, stillbirths, or severe illness in high-risk individuals.
Pregnant women, newborns, and people with weakened immune systems are at higher risk from Listeria monocytogenes. Most consumers are less likely to be affected.
Check for the UPC code 0-91404-15162-7 on the product packaging. The affected products are Premium Sorbet Quart, Trio, and Vanilla Strawberry Mango in 1-pack sizes.
Look for the UPC code 0-91404-15162-7 on the packaging to identify affected items.
The recall states the products may be contaminated with Listeria monocytogenes, so they are not safe to consume. Consumers should check the UPC code and follow the recall instructions.
Check the UPC code 0-91404-15162-7 on the packaging. The affected products are Premium Sorbet Quart, Trio, and Vanilla Strawberry Mango in 1-pack sizes.
The recall does not specify a remedy, so consumers should check the product UPC code and contact ICE CREAM HOUSE for further instructions.
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-1697-2023 — ICE CREAM HOUSE ICE CREAM HOUSE Hello, I own a ICE CREAM HOUSE that is covered by recall F-1697-2023 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.
