Snoqualmie Gourmet Ice Cream's Cherry Vanilla Custard (no egg) from January 2014 to December 2014 may contain Listeria monocytogenes. Consumers should check product dates and contact the company for details.
Cherry Vanilla Custard (without egg) is being recalled due to the potential to be contaminated with Listeria monocytogenes.
Snoqualmie Gourmet Ice Cream is recalling Cherry Vanilla Custard (without egg) due to potential Listeria monocytogenes contamination. This could 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. The ice cream was produced from January 1, 2014 to December 15, 2014 and may have been contaminated during manufacturing.
Pregnant women, newborns, and people with weakened immune systems are at higher risk from Listeria contamination. Anyone who purchased this ice cream between January 1, 2014 and December 15, 2014 is likely affected.
Check for Snoqualmie brand Cherry Vanilla Custard in 1.5 or 3-gallon plastic tubs. The product was sold between January 1, 2014 and December 15, 2014. No UPC number is listed.
Look for production dates on the tub between January 1, 2014 and December 15, 2014.
Reach out to Snoqualmie Gourmet Ice Cream for further instructions on how to handle the product.
The product may contain Listeria monocytogenes, which can cause serious illness. Do not consume until you get official guidance from Snoqualmie Gourmet Ice Cream.
Pregnant women, newborns, and people with weakened immune systems are at higher risk from Listeria contamination.
Check for Snoqualmie brand Cherry Vanilla Custard in 1.5 or 3-gallon plastic tubs with production dates from January 1, 2014 to December 15, 2014.
We’ve drafted a message you can send Snoqualmie to request your refund or repair — edit it as you like.
Subject: Recall F-1469-2015 — Snoqualmie Snoqualmie Hello, I own a Snoqualmie that is covered by recall F-1469-2015 from Snoqualmie. 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.
