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Lower risk Food recall · FDA · Published May 27, 2026

Produce Innovations: Incorrect Turkey/Cheddar Label on Roast Beef Sandwiches

Produce Innovations recalls roast beef and cheddar sandwiches labeled as turkey and cheddar due to incorrect product labeling. Consumers should check for green adhesive labels with specific text.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #H-1111-2026FoodProduce Innovations ›
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Contact the company

Recalling firmProduce Innovations1845 Colonial Pkwy · Norwalk, IA 50211-9742
✎ GovInfoNow plain-language explainer

Produce Innovations is recalling roast beef and cheddar sandwiches that were mistakenly labeled as turkey and cheddar. This could lead to confusion about the actual contents, potentially causing incorrect dietary choices or safety issues if the product is used for a different purpose. Read more at govinfonow.com/recall/6199-produce-innovations-incorrect-turkey-cheddar-label-on-roast-beef-sandwiches.

Source Summary by GovInfoNow · govinfonow.com/recall/6199-produce-innovations-incorrect-turkey-cheddar-label-on-roast-beef-sandwiches · Updated August 6, 2026 · Official notice: FDA #H-1111-2026

Cite this page

“Produce Innovations: Incorrect Turkey/Cheddar Label on Roast Beef Sandwiches.” GovInfoNow, updated August 6, 2026. https://govinfonow.com/recall/6199-produce-innovations-incorrect-turkey-cheddar-label-on-roast-beef-sandwiches. Based on FDA recall #H-1111-2026.

The FDA announced on May 27, 2026, that Produce Innovations voluntarily recalled roast beef and cheddar closed face sandwiches due to incorrect product labeling. The hazard involves the mislabeling of the contents as turkey and cheddar. Owners should discard the product or return it for a refund.

How to tell if you have it

  • Brand: Produce Innovations
  • Product: Roast beef and cheddar closed face sandwich
  • Label text: *Lunch Box Kitchen* Premium Convenience***Turkey & Cheddar Sub***BEST BY 06/14/26 Lot no. 26 134 NET WEIGHT: 6.1oz***KEEP REFRIGERATED*** Produced by: Produce Innovations***1845 Colonial Parkway Norwalk, IA 50211***
  • Lot code: 26134
  • Quantity: 112 individual units
  • Distribution: Medical facilities and vending distributors in IL, IA, KS and MO

The hazard

The roast beef and cheddar closed face sandwich was incorrectly labeled as a turkey and cheddar sub sandwich. This mislabeling poses an allergy risk to consumers with turkey allergies. The FDA has classified this recall as Class III.

How to tell if you have this one

Look for sandwiches in clear plastic wrap with a green adhesive label that says 'Turkey & Cheddar Sub' in the label text. The label also includes a lot code of 26134 and a best by date of 06/14/26.

  • Brand
    Produce Innovations
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Label

    Verify the label for the text 'Turkey & Cheddar Sub' and lot code 26134.

Where it went and when

Where it was distributed

Distributed in 4 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: yesIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: yesMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: yesKSArkansas: 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: “Medical facilities and vending distributors located in IL, IA, KS and MO” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Illinois, Iowa, Kansas, Missouri.

Recall timeline

FDA terminated this recall 40 days after the firm started it.

1. Firm started the recall: May 27, 202612. FDA classified it Class III: Jun 24, 202623. Published in FDA’s Enforcement Report: Jul 1, 202634. FDA terminated the recall: Jul 6, 202642026
  1. Firm started the recall
  2. FDA classified it Class III
  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.

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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 #H-1111-2026 (May 27, 2026)
  • Plain-language summary written by qwen3:4b on August 6, 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