FDA recall record

Delta Fresh LLC Product is a whole, fresh cucumber with no individual recall — FDA F-0372-2025

Potential Salmonella contamination of fresh cucumbers. Associated with an outbreak.

Class Iclassification
F-0372-2025official record ID
Jan 8, 2025report date

Recall record at a glance

Official recordF-0372-2025
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmDelta Fresh LLC.
Report dateJan 8, 2025
Recall initiation dateNov 27, 2024
Quantity6930 cases
LocationNogales, AZ, United States

Official product description

Product is a whole, fresh cucumber with no individual packaging, labeling, PLU, or other identifying information. Cucumber weight and size varies. Type of master packaging: 1.PACKAGED IN BULK IN 1 1/9 BUSHEL CARDBOARD BOXES WITH THE DELTA FRESH LABEL; OR 2.PACKAGED IN BULK IN 1 1/9 BUSHEL GENERIC WHITE CARDBOARD BOXES WITH A STICKER THAT PROVIDES THE IMPLICATED GROWER S NAME, AGROTATO, S.A. DE C.V. Net wt: 50 lb UPC: N/A Firm Name & Address listed on label: AGROTATO SA DE CV, BLVD. FRANCISCO EUSEBIO KINO NO. 315, INT. 706, COL. LOMAS DEL PITIC, C.P. 83010, HERMOSILLO, SONORA, MEXICO is listed on the master case. There is no packaging/label/sticker on the cucumbers

Why the product was recalled

Potential Salmonella contamination of fresh cucumbers. Associated with an outbreak.

Distribution information

Recalled product was distributed to the following states: AZ, CA, IL, MD, MI, MN, NY. and TX.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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