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PRIMO NO. 1 IN PRODUCE, INC recall - Cucumbers Peeled/Dice 1/4" KBS 5LB, Cardboard boxes
FDA (enforcement) · September 24, 2025 · Class I
- PRIMO NO. 1 IN PRODUCE, INC recalled Cucumbers Peeled/Dice 1/4" KBS 5LB, Cardboard boxes - an FDA enforcement event posted , classified Class I, covering 5 product entries.
- FDA-stated reason: Product contaminated with Salmonella
- Details as of ; the linked official notice is authoritative for lot codes, VINs, and remedies.
- Agency
- FDA
- Posted
- Initiated
- Classification
- Class I
- Status
- Terminated
- Recalling firm
- PRIMO NO. 1 IN PRODUCE, INC
- Source ID
- 96968
FDA Enforcement Report search →
How this recall compares
- No other recall event under the name Primo No. 1 In Produce, Inc appears in the FDA (2012+) and USDA-FSIS (2014+) records tracked here.
- It covers 5 product entries; 88% of the 574 FDA enforcement events posted in 2025 covered fewer.
- It is one of 3 Salmonella recall events FDA and USDA-FSIS posted in September 2025 (all Salmonella recalls).
Product entries (5)
| Recall # | Product | Codes / lots | Distribution |
|---|---|---|---|
| H-0606-2025 | Cucumbers Peeled/Dice 1/4" KBS 5LB, Cardboard boxes | X3232062 X3234353 X3235434 X3236030 | The recalled product was distributed to the following… |
| H-0607-2025 | Cucumber Peeled Sliced KBS 2/5lb, Cardboard Boxes | X3235434 | The recalled product was distributed to the following… |
| H-0608-2025 | Cucumber Sliced PLD ¿ KBS 2/10lb, Cardboard Boxes | X3234937 | The recalled product was distributed to the following… |
| H-0609-2025 | Vegetable Tray Cucumbers 3/2lb, Cardboard boxes | X3232225 X3233832 X3234937 X3231117 X3232225 X3233832 X3236030 X3232225 X3235440 X3236030… | The recalled product was distributed to the following… |
| H-0610-2025 | Cucumber Sliced 8oz 8ct/4#AV, Cardboard Boxes | X3231692 X3233832 X3234937 X3231117 X3233832 X3236030 X3231117 X3235434 X3231117 X3235434… | The recalled product was distributed to the following… |
FDA enforcement entries have no per-recall public URL - verify via the FDA Enforcement Report search using the firm name or a recall number above.
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