RecallHawk
Class III Recall

Roast beef and cheddar closed face sandwich packed in clear plastic wrap with a green adhesive label. The label reads in

Produce Innovations

Summary

The FDA issued a Class III for Roast beef and cheddar closed face sandwich packed in clear plastic wrap with a by Produce Innovations. Reason: Incorrect Product Label; Roast Beef and Swiss closed face sub sandwich labeled as Turkey and Cheddar closed face sub sandwich.

Details

Source

Food Recall

External ID

H-1111-2026

Action Date

2026-07-01

Status

Ongoing

Category

food

Product Description

Roast beef and cheddar closed face sandwich packed in clear plastic wrap with a green adhesive label. The label reads in part as "***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 Info: Lot code: 26134

Quantity Affected: 112 individual units

Reason for Recall

Incorrect Product Label; Roast Beef and Swiss closed face sub sandwich labeled as Turkey and Cheddar closed face sub sandwich

Distribution

Medical facilities and vending distributors located in IL, IA, KS and MO

Type: Voluntary: Firm initiated

Recall Initiated: 2026-05-27

Company

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 58 food recalls issued in the same week, part of 92 food-related FDA actions this month.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Produce Innovations) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Produce Innovations have FDA actions?

This is the only FDA action we have on record for Produce Innovations in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-1111-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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