← FDA ENFORCEMENT
F-0602-2024Class III
E.A. Sween Co.
What this record is not
A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.
Recalling firm
E.A. Sween Co.
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2023-12-20
Distribution
CA, CO, CT, FL, GA, ID, IL, LA, MD, MI, MN, MO, NJ, OR, PA, SD, TN, TX, WI
Firm state
MN
Product quantity
3,155 cases (31,550 eaches)
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Documentation & Change ControlReason for recall
Label mix-up and therefore required label information is inaccurate
Product description
Deli Express, Deli Club 4.4oz wedge sandwich, 10 retail units per wholesale case, UPC 41433-00157
Code / lot info
lot code U023236
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See all Documentation & Change Control recalls →Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →