El Alteno Raisinettes Dovales 12 oz. Recall: Undeclared Milk and Soy Lecithin
El Alteno recalls 12 oz. Raisinettes Dovales with undeclared milk and soy lecithin. Consumers should check UPC 8 20202 00411 4 for affected products.
Lower-risk recall
Undeclared milk and soy lecithin.
Contact the company
What happened, in plain English
El Alteno is recalling its Raisinettes Dovales 12 oz. product due to undeclared milk and soy lecithin. This could affect people with allergies to these ingredients. Read more at govinfonow.com/recall/23635-el-alteno-raisinettes-dovales-12-oz-recall-undeclared-milk-and.
Source Summary by GovInfoNow · govinfonow.com/recall/23635-el-alteno-raisinettes-dovales-12-oz-recall-undeclared-milk-and · Updated October 9, 2026 · FDA enforcement record: FDA #F-2343-2016
Cite this page
“El Alteno Raisinettes Dovales 12 oz. Recall: Undeclared Milk and Soy Lecithin.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23635-el-alteno-raisinettes-dovales-12-oz-recall-undeclared-milk-and. Based on FDA recall #F-2343-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2343-2016%22&limit=1).
Why it’s dangerous
The product contains undeclared milk and soy lecithin, which can cause allergic reactions in sensitive individuals. This is a food safety issue for those with allergies to these ingredients.
Who’s affected
People with milk or soy allergies may be affected. The recall applies to consumers who purchased the specific product with UPC 8 20202 00411 4.
How to tell if you have this one
Check for the product name 'El Alteno Raisinettes Dovales 12 oz.' with UPC 8 20202 00411 4. The expiration date is 06/30/2017.
- Brand
El Alteno- Product
El Alteno Raisinettes Dovales 12 oz. UPC: 8 20202 00411 4- Category
Food
What to do — step by step
Check Product Details
Look for the UPC code 8 20202 00411 4 on the product label.
Where it went and when
Where it was distributed
Distributed in 3 states.
FDA distribution: “U.S. distribution to the following; CA, AZ, NV. No foreign distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, California, Nevada.
Recall timeline
FDA terminated this recall 9 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
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-2343-2016 (August 5, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2343-2016 to see it in context.
- Plain-language summary written by qwen3:4b on October 9, 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.