Fresh Recalls

FDAClass III · Food · Recall H-1111-2026 · Recalled July 1, 2026

Roast beef and cheddar closed face sandwich packed in clear plastic wrap with a green adhe recall — Produce Innovations

Agency report date: July 1, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Roast beef and cheddar closed face sandwich packed in clear plastic wrap with a green adhe
Company / brand
Produce Innovations
Lot / serial / date codes
Lot code: 26134
Distribution
Medical facilities and vending distributors located in IL, IA, KS and MO
Agency product description and boundaries

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***"

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

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

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class III: not likely to cause adverse health consequences.

Affected product: Roast beef and cheddar closed face sandwich packed in clear plastic wrap with a green adhe

3. Open the official notice or contact

Official recall ID
H-1111-2026
Brand
Produce Innovations
Classification
Class III
Units affected
112 individual units
Recall status
Terminated
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Norwalk, IA, United States
Firm address
1845 Colonial Pkwy, N/A, 50211-9742

Identifying details (verbatim from the notice)

Product codes / lots
Lot code: 26134
Distribution
Medical facilities and vending distributors located in IL, IA, KS and MO
Firm notified the public via
Telephone
FDA event ID
99099
Recall initiated
May 27, 2026
FDA classified
June 24, 2026
FDA report date
July 1, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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