Class ITerminatedVoluntary: Firm initiated
Delta Fresh LLC.: food recall F-0372-2025
Delta Fresh LLC. of Nogales, AZ recalled Product is a whole, fresh cucumber with no individual packaging, labeling, PLU, or other identifying information.… Reason: Potential Salmonella contamination of fresh cucumbers. Associated with an outbreak. The FDA listed it as Class I in its Enforcement Report dated Jan 8, 2025; distribution: Arizona, California, Illinois, Maryland, Michigan, Minnesota, New York, Texas.
Record status as published: Terminated (terminated Apr 10, 2025). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 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
- Product quantity
- 6930 cases
- Reason for recall
- Potential Salmonella contamination of fresh cucumbers. Associated with an outbreak.
- Codes, lots and dates on the package
- Delta Fresh does NOT assign lot information to the shipping container.
- Distribution pattern
- Recalled product was distributed to the following states: AZ, CA, IL, MD, MI, MN, NY. and TX.
- Recalling firm
- Delta Fresh LLC., Nogales, AZ
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Nov 27, 2024 |
| Classified by the FDA | Jan 2, 2025 |
| Published in the Enforcement Report | Jan 8, 2025 |
| Terminated | Apr 10, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0372-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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