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Lower risk Food recall · FDA · Published May 11, 2017

Red Robin Burgers and Brews Crispy Onion Rings Recall: Undeclared Milk Hazard

Lamb Weston recalls 14oz frozen Red Robin Burgers and Brews Crispy Onion Rings due to undeclared milk. Consumers should check UPC 043301611193 for affected products.

🇺🇸 FDA recall #F-2337-2017FoodLamb Weston ›
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Recalling firmLamb Weston Inc8701 W Gage Blvd · Kennewick, WA 99336-1034
✎ GovInfoNow plain-language explainer

What happened, in plain English

Lamb Weston is recalling 14-ounce frozen Red Robin Burgers and Brews Crispy Onion Rings because they contain undeclared milk. This poses a risk for people with milk allergies who may experience allergic reactions if they consume the product. Read more at govinfonow.com/recall/21362-red-robin-burgers-and-brews-crispy-onion-rings-recall-undeclared.

Source Summary by GovInfoNow · govinfonow.com/recall/21362-red-robin-burgers-and-brews-crispy-onion-rings-recall-undeclared · Updated October 8, 2026 · FDA enforcement record: FDA #F-2337-2017

Cite this page

“Red Robin Burgers and Brews Crispy Onion Rings Recall: Undeclared Milk Hazard.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21362-red-robin-burgers-and-brews-crispy-onion-rings-recall-undeclared. Based on FDA recall #F-2337-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2337-2017%22&limit=1).

Why it’s dangerous

The product contains undeclared milk, meaning it's not listed as an ingredient on the label. This can cause allergic reactions in individuals who are sensitive or allergic to milk. The hazard is specific to those with milk allergies and does not pose a general safety risk.

Who’s affected

People with milk allergies are most at risk from consuming these products. The recall affects consumers who purchased the frozen burgers and onion rings with the specific UPC code.

How to tell if you have this one

Check for the UPC code 043301611193 on the retail package. The product was sold between October 28 and October 29, 2018, and is labeled as 14 ounces frozen.

  • Brand
    Lamb Weston
  • Product
    Red Robin Burgers and Brews Crispy Onion Rings, frozen, Net wt. 14 ounce. Retail package UPC 0 43301 61119 3
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the UPC code 043301611193 on the retail package of the frozen product.

Where it went and when

Where it was distributed

Distributed in 19 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: yesMNIllinois: yesILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: yesOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: yesTXFlorida: not listedFL

FDA distribution: “distributed in AR, AZ, CA, CO, IL, KS, KY, MN, MO, NE, NM, NV, OK, OR, TN, TX, UT, WA, and WY.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, Arkansas, California, Colorado, Illinois, Kansas, Kentucky, Minnesota, Missouri, Nebraska, Nevada, New Mexico, Oklahoma, Oregon, Tennessee, Texas, Utah, Washington, Wyoming.

Recall timeline

FDA terminated this recall 3 months after the firm started it.

1. Firm started the recall: May 11, 201712. FDA classified it Class I: Jun 7, 201723. Published in FDA’s Enforcement Report: Jun 14, 201734. FDA terminated the recall: Aug 15, 201742017
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

Is there a risk of serious injury from this product?

No, the recall is for people with milk allergies. There is no risk of serious injury to the general public.

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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-2337-2017 (May 11, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2337-2017 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA