Recall record at a glance
| Official record | F-0373-2025 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | BALOIAN FARMS |
| Report date | Jan 8, 2025 |
| Recall initiation date | Nov 29, 2024 |
| Quantity | 40,043 cases |
| Location | Nogales, AZ, United States |
Official product description
whole fresh American cucumbers packaged in bulk cardboard containers labeled with the "Pamela" brand, a generic white box with a sticker that provides the implicated grower's name, "Agrotato, S.A. de C.V.," or a clear PamPak branded bag of 6 individual cucumbers with the UPC 8 2540107010 6 " Pamela (Bulk Pack 24ct, 36ct, Small, Large, Plain, Select and Super Select) Distributed to Wholesale, Food Service, Retail, and Brokers " Stock "Vegetables" (Bulk Pack 24ct, 36ct, Small, Large, Plain, Select and Super Select) Distributed to Wholesale, Food Service, Retail and Brokers " PamPak (6x6 Bagged Cucumbers) with UPC code:825401070106 Distributed to 2 Wholesale distributers (3 locations) Pamela (24 Ct, 36 Ct, Plain, Large, Select, Super Select, Small) Stock Vegetables (Plain, Large, Select, Super Select, Small) PamPak (6x6ct Bag Pack) Case Label GTIN: 10825401300514
Why the product was recalled
Cucumbers potentially contaminated with Salmonella.
Distribution information
Distributed to the following states: AK, AZ, CA, CO, IA, ID, KS, MA, MI, MO, MT, NV, NY, NC, OR, TX, WA, and WI.
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
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
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