Snoqualmie Gourmet Ice Cream recalls Berry Ripple Sorbet (1.5-gallon tubs) produced Jan 2014-Dec 2014 due to potential Listeria monocytogenes contamination. Consumers should avoid consumption.
Berry Ripple Sorbet is being recalled due to the potential to be contaminated with Listeria monocytogenes
Snoqualmie Gourmet Ice Cream is recalling Berry Ripple Sorbet sold in 1.5-gallon plastic tubs from January 1, 2014 through December 15, 2014. The product may contain Listeria monocytogenes, a bacteria that can cause serious illness.
Listeria monocytogenes is a bacteria that can cause serious infections, especially in pregnant women, newborns, and people with weakened immune systems. Contaminated food can lead to illness if consumed.
Anyone who purchased Snoqualmie Berry Ripple Sorbet between January 1, 2014 and December 15, 2014. People with weakened immune systems are at higher risk of infection.
Look for Snoqualmie Berry Ripple Sorbet in 1.5-gallon plastic tubs. The product was produced between January 1, 2014 and December 15, 2014. There is no UPC code.
Verify the production date is between January 1, 2014 and December 15, 2014.
If the product was produced during the recall period, discard it immediately.
No, the product may contain Listeria monocytogenes, which can cause serious illness. Do not consume.
Look for Snoqualmie Berry Ripple Sorbet in 1.5-gallon plastic tubs produced between January 1, 2014 and December 15, 2014. There is no UPC code.
The recall does not provide a specific remedy. Consumers should discard the product if it was produced during the recall period.
We’ve drafted a message you can send Snoqualmie to request your refund or repair — edit it as you like.
Subject: Recall F-1493-2015 — Snoqualmie Snoqualmie Hello, I own a Snoqualmie that is covered by recall F-1493-2015 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.
