Zarlengo's Double Dark Chocolate Gelato in 1-gallon buckets may have soy listed in ingredients but not in contains statement. Consumers should check lot codes for affected batches.
Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.
Zarlengo's Double Dark Chocolate Gelato in 1-gallon buckets is being recalled because soy lecithin is listed in the ingredients but not in the 'contains' statement. This could lead to confusion about soy content for consumers with allergies.
The product lists soy lecithin in the ingredients but does not mention soy in the 'contains' statement. This could mislead consumers with soy allergies into thinking the product is soy-free when it might contain soy.
People who purchased Zarlengo's Double Dark Chocolate Gelato in 1-gallon buckets with lot codes 05726 are affected. Those with soy allergies may be at higher risk due to potential mislabeling.
Check for 1-gallon buckets with lot code 05726. The product is labeled as white round food and freezer grade with a tamper-resistant lid.
Look for lot code 05726 on the 1-gallon bucket/pail of Zarlengo's Double Dark Chocolate Gelato.
The recall indicates soy lecithin is listed in ingredients but not in the contains statement, which could mean soy is present. Consumers with soy allergies should check if they have the affected lot code.
Lot code 05726 for 1-gallon buckets. Other lot codes include 00226, 03026, 05426, and 33825 for smaller sizes.
Check for 1-gallon buckets with lot code 05726. The product is white round food and freezer grade with a tamper-resistant lid.
We’ve drafted a message you can send Zarl:engo to request your refund or repair — edit it as you like.
Subject: Recall H-0652-2026 — Zarl:engo Zarl:engo Hello, I own a Zarl:engo that is covered by recall H-0652-2026 from Zarl:engo. 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.
