Reser's Fine Foods Macaroni Salad Recall: Undeclared Milk and Soy
Reser's Fine Foods recalls American Classics Macaroni Salad due to undeclared milk and soy. Consumers should check UPC 7117.19007 for affected products.
Lower-risk recall
Product contains undeclared milk and soy.
Contact the company
What happened, in plain English
Reser's Fine Foods is recalling American Classics Macaroni Salad because it contains undeclared milk and soy. This could cause allergic reactions in people with milk or soy allergies. Read more at govinfonow.com/recall/21898-reser-s-fine-foods-macaroni-salad-recall-undeclared-milk-and.
Source Summary by GovInfoNow · govinfonow.com/recall/21898-reser-s-fine-foods-macaroni-salad-recall-undeclared-milk-and · Updated October 8, 2026 · FDA enforcement record: FDA #F-2203-2017
Cite this page
“Reser's Fine Foods Macaroni Salad Recall: Undeclared Milk and Soy.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21898-reser-s-fine-foods-macaroni-salad-recall-undeclared-milk-and. Based on FDA recall #F-2203-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2203-2017%22&limit=1).
Why it’s dangerous
The product contains undeclared milk and soy, which can cause allergic reactions in sensitive individuals. This is a food safety issue related to ingredient labeling.
Who’s affected
People with milk or soy allergies are at risk. The product is sold in 16 oz plastic tubs with UPC 7117.19007.
How to tell if you have this one
Check for the UPC 7117.19007 on the product label. The product is sold in 16 oz plastic tubs, 12 per case, with a use-by date of April 24, 2017.
- Brand
Reser's Fine Foods- Category
Food
What to do — step by step
Check Product Label
Look for the UPC 7117.19007 on the 16 oz plastic tub.
Where it went and when
Where it was distributed
Distributed in 12 states.
FDA distribution: “Product was distributed to wholesalers for retail sale: AL, CO, GA, KS, MO, MS, NY, OK, LA, PA, TX, WI. There was no foreign/government/military distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Colorado, Georgia, Kansas, Louisiana, Mississippi, Missouri, New York, Oklahoma, Pennsylvania, Texas, Wisconsin.
Recall timeline
FDA terminated this recall 2 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- 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-2203-2017 (March 31, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2203-2017 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.