McCain Foods USA: Frozen Onion Rings Lacking Milk Label Recall
McCain Foods USA recalls frozen onion rings sold under multiple private labels that do not declare milk on the label. This may affect consumers who require milk labeling for dietary needs.
Lower-risk recall
Product label does not declare milk.
Contact the company
What happened, in plain English
McCain Foods USA is recalling frozen onion rings sold under several private labels because the product label does not declare milk. This could be a problem for people with dietary restrictions that require milk labeling. Read more at govinfonow.com/recall/23132-mccain-foods-usa-frozen-onion-rings-lacking-milk-label-recall.
Source Summary by GovInfoNow · govinfonow.com/recall/23132-mccain-foods-usa-frozen-onion-rings-lacking-milk-label-recall · Updated October 9, 2026 · FDA enforcement record: FDA #F-0433-2017
Cite this page
“McCain Foods USA: Frozen Onion Rings Lacking Milk Label Recall.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23132-mccain-foods-usa-frozen-onion-rings-lacking-milk-label-recall. Based on FDA recall #F-0433-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0433-2017%22&limit=1).
Why it’s dangerous
The product label does not declare milk, which could be a problem for individuals with dietary restrictions that require milk labeling. This is a labeling issue rather than a safety hazard.
Who’s affected
People who purchased frozen onion rings from the listed private labels between October 20, 2015 and September 23, 2016 are likely affected. Those with dietary needs requiring milk labeling on food products are at higher risk.
How to tell if you have this one
Check for frozen onion rings with private labels: Premium Pick 5 Mix and Match, Krasdale, Spartan, Shur Fine, Kroger, or Fareway Breaded. Look for production date codes from V151020 to V160923.
- Brand
McCain Foods USA- Category
Food
What to do — step by step
Check Label for Milk Declaration
Look for a milk declaration on the product label. If it is missing, the product is part of the recall.
Where it went and when
Where it was distributed
Distributed in 23 states.
FDA distribution: “Recalled product was distributed to direct accounts in AL, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MD, MI, MO, NC, NE, NY, OH, TN, TX, VA, and WI” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Colorado, Connecticut, Florida, Georgia, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maryland, Michigan, Missouri, Nebraska, New York, North Carolina, Ohio, Tennessee, Texas, Virginia, Wisconsin.
Recall timeline
FDA terminated this recall 7 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-0433-2017 (September 23, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0433-2017 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.