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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Low RiskFDA Food
Food & Beverages/Packaged & Processed

Deli Express Deli Club Wedge Sandwich Recalled for Inaccurate Label Information

Agency Publication Date: December 14, 2023
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Summary

E.A. Sween Co. is recalling approximately 31,550 units (3,155 cases) of Deli Express Deli Club 4.4oz wedge sandwiches because of a label mix-up that caused required product information to be inaccurate. No incidents or injuries have been reported to date. Consumers should return the product to the place of purchase for a refund or dispose of it.

Risk

A labeling error resulted in inaccurate required information on the product packaging, which could lead consumers to consume products without full knowledge of their contents or ingredients. No injuries have been reported in connection with this recall.

What You Should Do

  1. This recall affects Deli Express Deli Club 4.4oz wedge sandwiches with UPC 41433-00157 and lot code U023236.
  2. Return the product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls for additional information.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Deli Express Deli Club wedge sandwich (4.4oz)
UPC Codes:
41433-00157
Lot Numbers:
U023236

10 retail units per wholesale case; total quantity 3,155 cases (31,550 eaches).

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93571
Status: Resolved
Manufacturer: E.A. Sween Co.
Sold By: Retail units
Manufactured In: United States
Units Affected: 3,155 cases (31,550 eaches)
Distributed To: California, Colorado, Connecticut, Florida, Georgia, Idaho, Illinois, Louisiana, Maryland, Michigan, Minnesota, Missouri, New Jersey, Oregon, Pennsylvania, South Dakota, Tennessee, Texas, Wisconsin

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.