Velvet Ice Cream Company recalls Super Dip Vanilla and Orange 56oz cartons (4 per case) due to potential Listeria monocytogenes contamination. Consumers should avoid consumption of affected products.
Potentially contaminated with Listeria monocytogenes
Velvet Ice Cream Company is recalling Super Dip Vanilla and Orange ice cream in 56oz cartons (4 per case) because they may be contaminated with Listeria monoc: a bacteria that can cause serious illness. This recall is important because Listeria can lead to severe health issues, especially for pregnant women, newborns, and those with weakened immune systems.
Listeria monocytogenes is a bacteria that can cause serious infections, including miscarriages, stillbirths, and severe illness in newborns. It can also cause life-threatening infections in people with weakened immune systems. The ice cream may have been contaminated during production or handling.
Pregnant women, newborns, and people with weakened immune systems are most at risk from Listeria contamination. Anyone who has purchased the affected ice cream products should check if they have them.
Check for 56oz cartons labeled 'Super Dip Vanilla/Orange' with lot number 21106. The product comes in sets of 4 cartons per case.
Look for the lot number 21106 on the carton to confirm if it's affected.
The ice cream may be contaminated with Listeria monocytogenes, which can cause serious health issues. Do not consume the affected products.
Check for 56oz cartons labeled 'Super Dip Vanilla/Orange' with lot number 21106. The product comes in sets of 4 cartons per case.
Do not consume the affected products. Check the lot number on the carton to confirm if it's part of the recall.
We’ve drafted a message you can send Velvet Ice Cream Company to request your refund or repair — edit it as you like.
Subject: Recall F-0608-2021 — Velvet Ice Cream Company Velvet Ice Cream Company Hello, I own a Velvet Ice Cream Company that is covered by recall F-0608-2021 from Velvet Ice Cream Company. 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.
