RecallHawk
Class I Recall

Cucumbers Peeled/Dice 1/4" KBS 5LB, Cardboard boxes

PRIMO NO. 1 IN PRODUCE, INC

Summary

The FDA issued a Class I for Cucumbers Peeled/Dice 1/4" KBS 5LB, Cardboard boxes by PRIMO NO. 1 IN PRODUCE, INC. Reason: Product contaminated with Salmonella.

Details

Source

Food Recall

External ID

H-0606-2025

Action Date

2025-09-24

Status

Terminated

Category

food

Product Description

Cucumbers Peeled/Dice 1/4" KBS 5LB, Cardboard boxes

Lot/Code Info: X3232062 X3234353 X3235434 X3236030

Quantity Affected: 89 Cardboard Boxes (total)

Reason for Recall

Product contaminated with Salmonella

Distribution

The recalled product was distributed to the following states : VA, NY, PA, NJ

Type: Voluntary: Firm initiated

Recall Initiated: 2025-05-20

Company

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 51 food recalls issued in the same week, part of 204 food-related FDA actions this month.

PRIMO NO. 1 IN PRODUCE, INC has 5 FDA actions in our database, including 5 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (PRIMO NO. 1 IN PRODUCE, INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does PRIMO NO. 1 IN PRODUCE, INC have FDA actions?

PRIMO NO. 1 IN PRODUCE, INC has 5 FDA actions in our database, including 5 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0606-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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