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E.A. Sween Co. Recall: Label mix-up and therefore required label information is inaccurate

United States

TerminatedClass III

Company
E.A. Sween Co.
Product
Deli Express, Deli Club 4.4oz wedge sandwich, 10 retail unit…
Recall date
December 7, 2023
Terminated
February 29, 2024
Source
FDA

Reason for recall

Label mix-up and therefore required label information is inaccurate

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Deli Express, Deli Club 4.4oz wedge sandwich, 10 retail units per wholesale case, UPC 41433-00157 41433-00157 3,155 cases (31,550 eaches) lot code U023236

Distribution

  • CA
  • CO
  • CT
  • FL
  • GA
  • ID
  • IL
  • LA
  • MD
  • MI
  • MN
  • MO
  • NJ
  • OR
  • PA
  • SD
  • TN
  • TX
  • WI

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0602-2024
Event ID
93571
Status
Terminated
Classification
Class III
Company
E.A. Sween Co.
Product description
Deli Express, Deli Club 4.4oz wedge sandwich, 10 retail units per wholesale case, UPC 41433-00157
Quantity
3,155 cases (31,550 eaches)
Reason
Label mix-up and therefore required label information is inaccurate
Recall initiation date
December 7, 2023
Report date
December 20, 2023
Classification date
Not published in this source record
Termination date
February 29, 2024
Distribution pattern
CA, CO, CT, FL, GA, ID, IL, LA, MD, MI, MN, MO, NJ, OR, PA, SD, TN, TX, WI
UPC, lot, and code information
UPC 41433-00157; lot code U023236
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: E.A. Sween Co.

Other recalls from E.A. Sween Co.

FDA Recall United States Terminated Historical recordClass II

E.A. Sween Co.

Product
Deli Express BBQ Pulled Pork on a sesame bun. Net Wt 5.5oz…
Published
November 5, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

E.A. Sween Co.

Product
Market Sandwich Artisan Style Albacore Tuna Salad on Dark Wh…
Published
October 23, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

E.A. Sween Co.

Product
Tuna Salad on Wheat Bread, Keep Refrigerated. packaged un…
Published
October 23, 2019
Distribution
Nationwide

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Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
California 1
Colorado 1
Connecticut 1
Florida 1
Georgia 1
Idaho 1
Illinois 1
Louisiana 1
Maryland 1
Michigan 1
Minnesota 1
Missouri 1
New Jersey 1
Oregon 1
Pennsylvania 1
South Dakota 1
Tennessee 1
Texas 1
Wisconsin 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class III mean?

A situation in which use of or exposure to a product is not likely to cause adverse health consequences.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.