Rosa Foods Soylent 1.1 Powder Recall: Undeclared Milk Risk
Rosa Foods recalls Soyl: 1.8 Powder pouches for possible undeclared milk (whey) content. Consumers should check product details and contact Rosa Foods for guidance.
Lower-risk recall
Rosa Foods is recalling Soylent Bar because it may contain undeclared milk (whey).
Contact the company
What happened, in plain English
Rosa Foods is recalling Soylent 1.8 Powder pouches due to potential undeclared milk (whey) in the product. This could cause allergic reactions in people with milk allergies. The recall affects specific lot numbers sold until February 2018. Read more at govinfonow.com/recall/21820-rosa-foods-soylent-1-1-powder-recall-undeclared-milk-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/21820-rosa-foods-soylent-1-1-powder-recall-undeclared-milk-risk · Updated October 8, 2026 · FDA enforcement record: FDA #F-2184-2017
Cite this page
“Rosa Foods Soylent 1.1 Powder Recall: Undeclared Milk Risk.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21820-rosa-foods-soylent-1-1-powder-recall-undeclared-milk-risk. Based on FDA recall #F-2184-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2184-2017%22&limit=1).
Why it’s dangerous
The product may contain undeclared milk (whey), which can trigger allergic reactions in individuals with milk allergies. This is a food safety issue related to ingredient labeling.
Who’s affected
People who purchased Soylent 1.8 Powder pouches with SKU 1WK-V108 from Rosa Foods HQ. Those with milk allergies are at higher risk of allergic reactions.
How to tell if you have this one
Check for the SKU 1WK-V108 on the product label. The product was sold in 7 x 15oz pouches with lot number G7076PA and expired by February 2018.
- Brand
Rosa Foods- Category
Food
What to do — step by step
Check Product Details
Look for SKU 1WK-V108 on the product label to confirm if it's part of the recall.
How this recall unfolded
Recall timeline
FDA terminated this recall 17 days after the firm started it.
- Firm started the recall
- FDA classified it Class I
- FDA terminated the recall
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #F-2184-2017 (April 21, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2184-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.