Delta Fresh LLC. Recall: Potential Salmonella contamination of fresh cucumbers. Associated with an outbreak.
United States
TerminatedClass I
- Company
- Delta Fresh LLC.
- Product
- Product is a whole, fresh cucumber with no individual packag…
- Recall date
- November 27, 2024
- Terminated
- April 10, 2025
- Source
- FDA
Reason for recall
Potential Salmonella contamination of fresh cucumbers. Associated with an outbreak.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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 | Not published in this source record | 6930 cases | Delta Fresh does NOT assign lot information to the shipping container. |
Distribution
- Recalled product was distributed to the following states: AZ
- CA
- IL
- MD
- MI
- MN
- NY. and TX.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0372-2025
- Event ID
- 95872
- Status
- Terminated
- Classification
- Class I
- Company
- Delta Fresh LLC.
- 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
- Quantity
- 6930 cases
- Reason
- Potential Salmonella contamination of fresh cucumbers. Associated with an outbreak.
- Recall initiation date
- November 27, 2024
- Report date
- January 8, 2025
- Classification date
- Not published in this source record
- Termination date
- April 10, 2025
- Distribution pattern
- Recalled product was distributed to the following states: AZ, CA, IL, MD, MI, MN, NY. and TX.
- UPC, lot, and code information
- Delta Fresh does NOT assign lot information to the shipping container.
- 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: Delta Fresh LLC.
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.
| State | Distributed |
|---|---|
| Arizona | 1 |
| California | 1 |
| Illinois | 1 |
| Maryland | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| New York | 1 |
| Texas | 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.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
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 I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
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.
