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Use caution Food recall · FDA · Published August 14, 2016

Supermom's Roast Beef Recall: Undeclared Allergens

Northern Tier Bakery recalls Supermom's Kitchen Roast Beef & Cheddar Melt due to mislabeling that omits monosodium glutamate, yellow 5, and yellow 6.

🇺🇸 FDA recall #F-0069-2017FoodSupermom's Kitchen ›
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Contact the company

Recalling firmNorthern Tier Bakery625 2nd St · St Paul Park, MN 55071-1807
✎ GovInfoNow plain-language explainer

What happened, in plain English

Northern Tier Bakery is recalling one lot of Supermom’s Kitchen Roast Beef & Cheddar Melt because the packaging was mislabeled. The product failed to declare the presence of monosodium glutamate, yellow 5, and yellow 6. This matters because consumers with allergies or sensitivities to these ingredients may be exposed without knowing. Read more at govinfonow.com/recall/23457-supermom-s-roast-beef-recall-undeclared-allergens.

Source Summary by GovInfoNow · govinfonow.com/recall/23457-supermom-s-roast-beef-recall-undeclared-allergens · Updated October 11, 2026 · FDA enforcement record: FDA #F-0069-2017

Cite this page

“Supermom's Roast Beef Recall: Undeclared Allergens.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/23457-supermom-s-roast-beef-recall-undeclared-allergens. Based on FDA recall #F-0069-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0069-2017%22&limit=1).

Why it’s dangerous

The product contains ingredients that were not listed on the label. This poses a risk to people who rely on ingredient lists to avoid allergens or specific food dyes and additives.

Who’s affected

Consumers in Wisconsin and Minnesota who purchased Supermom’s Kitchen Roast Beef & Cheddar Melt with UPC 63913-94236 and an Enjoy Through date of 8/19. Individuals allergic to or sensitive to monosodium glutamate, yellow 5, or yellow 6 are at risk.

How to tell if you have this one

Check for Supermom’s Kitchen Roast Beef & Cheddar Melt, Net Wt. 3.7 oz (105g). Look for the UPC 63913-94236 and an Enjoy Through date of 8/19. The product should be kept refrigerated.

  • Brand
    Supermom's Kitchen
  • Product
    Supermom s Kitchen Roast Beef & Cheddar Melt, Net Wt. 3.7 oz (105g). Keep Refrigerated. UPC 63913-94236
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check your product

    Verify if you have the recalled item by checking the UPC 63913-94236 and Enjoy Through date of 8/19.

  2. Do not consume

    If you have the mislabeled product, do not eat it due to the undeclared ingredients.

Where it went and when

Where it was distributed

Distributed in Minnesota and Wisconsin.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: yesMNIllinois: not listedILWisconsin: yesWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “Wisconsin and Minnesota.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Minnesota, Wisconsin.

Recall timeline

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

1. Firm started the recall: Aug 14, 201612. FDA classified it Class II: Oct 7, 201623. Published in FDA’s Enforcement Report: Oct 19, 201634. FDA terminated the recall: Aug 22, 2019420162019
  1. Firm started the recall
  2. FDA classified it Class II
  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

Where was this product sold?

The recalled units were distributed in Wisconsin and Minnesota.

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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-0069-2017 (August 14, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0069-2017 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 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