FDA recall, , Low risk
Lunch Box Kitchen Roast Beef and Cheddar Closed Face Sandwich
Roast beef and cheddar closed face sandwich is mislabeled as Turkey and Cheddar sub.
Recall ended Jul 6, 2026. Still check yours.
Summary by Recall Canary from the FDA notice
What happened
Produce Innovations, of Norwalk, Iowa, recalled 112 individual units of its Roast beef and cheddar closed face sandwich because of an incorrect product label. The sandwich, packed in clear plastic wrap with a green adhesive label, is labeled as a Turkey and Cheddar sub, but it contains roast beef and Swiss. The recall began on May 27, 2026, and was added to the FDA's Enforcement Report on June 24, 2026.
The product was distributed to medical facilities and vending distributors in Illinois, Iowa, Kansas, and Missouri. The label reads in part as Lunch Box Kitchen Premium Convenience Turkey and Cheddar Sub with a best by date of 06/14/26, keep refrigerated, produced by Produce Innovations at 1845 Colonial Parkway Norwalk, IA 50211.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for food recalls:
- Return it to the store where you bought it, or throw it away.
- Don't give it to anyone else, such as a food bank, or to a pet.
Is yours affected?
Match the best-by date and lot code listed under your product.
Roast beef and cheddar closed face sandwich
- Best-by date
- 06/14/26
- Lot code
- 26 134
From the FDA notice
Roast beef and cheddar closed face sandwich packed in clear plastic wrap with a green adhesive label.
Recall details
- Company began the recall
- Company
- Produce InnovationsNorwalk, Iowa
- Hazard
- Labeling error
- Risk
Low risk
Eating it is unlikely to cause health problems.
FDA Class III recall · How risk is rated
- Event ID
- 99099
- Recall number
- H-1111-2026
- Quantity recalled
- 112 individual units
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Recall ended
Archived
Summary updated
