CLASS I Food recall · Reported 8 Jan 2025 · FDA Enforcement Report

whole fresh American cucumbers recalled by Baloian Farms

Baloian Farms is recalling whole fresh American cucumbers, distributed in 18 states. The recall was initiated on 29 Nov 2024 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesNo codes or PLU labels are applied to individual cucumbers. Lot Number (Master Case) Qty (Cases) Ship Date 3-58614 71 cases 10/25/2024 3-58642 180 cases 10/18/2024 3-28729 16 cases 10/24/2024 3-58857 64 cases 11/01/2024 3-58866 70 cases 11/04/2024 3-58891 162 cases 11/05/2024 3-58919 14 cases 10/07/2024 3-58943 92 cases 11/08/2024 3-58984 34 cases 11/12/2024 3-59020 42 cases 11/12/2024 The consumer bag has a UPC code of: 825401070106
Quantity recalled40,043 cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0373-2025
FDA event ID
95873
Recalling firm
Baloian Farms, Nogales, AZ
Classification
Class I
Status
Terminated
Recall initiated
29 Nov 2024
FDA classified
2 Jan 2025
Reported
8 Jan 2025
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Salmonella
Product category
Fish

Timeline

29 Nov 2024Recall initiated by company
2 Jan 2025Classified by FDA+34 days
8 Jan 2025Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Cucumbers potentially contaminated with Salmonella.

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

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

Where it was distributed

Distributed to the following states: AK, AZ, CA, CO, IA, ID, KS, MA, MI, MO, MT, NV, NY, NC, OR, TX, WA, and WI.

AlaskaArizonaCaliforniaColoradoIowaIdahoKansasMassachusettsMichiganMissouriMontanaNorth CarolinaNevadaNew YorkOregonTexasWashingtonWisconsin

Questions about this recall

Why was it recalled?

Cucumbers potentially contaminated with Salmonella.

Which lots are affected?

No codes or PLU labels are applied to individual cucumbers. Lot Number (Master Case) Qty (Cases) Ship Date 3-58614 71 cases 10/25/2024 3-58642 180 cases 10/18/2024 3-28729 16 cases 10/24/2024 3-58857 64 cases 11/01/2024 3-58866 70 cases 11/04/2024 3-58891 162 cases 11/05/2024 3-58919 14 cases 10/07/2024 3-58943 92 cases 11/08/2024 3-58984 34 cases 11/12/2024 3-59020 42 cases 11/12/2024 The consumer bag has a UPC code of: 825401070106

Where was it sold?

Distributed to the following states: AK, AZ, CA, CO, IA, ID, KS, MA, MI, MO, MT, NV, NY, NC, OR, TX, WA, and WI.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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