RecallHawk
Class I Recall

Cucumber 24 Ct Repacked by Lipman Produce Hendersonville, NC 28792, Product of USA

LIPMAN FAMILY FARMS

Summary

The FDA issued a Class I for Cucumber 24 Ct Repacked by Lipman Produce Hendersonville, NC 28792, Product of U by LIPMAN FAMILY FARMS. Reason: Potential Salmonella Contamination.

Details

Source

Food Recall

External ID

H-0026-2025

Action Date

2025-06-18

Status

Terminated

Category

food

Product Description

Cucumber 24 Ct Repacked by Lipman Produce Hendersonville, NC 28792, Product of USA

Lot/Code Info: Expiration date: 5/14/2025-5/23/2025 Lot numbers# 3-431775 3-431809 3-431847 3-431899 3-431919 3-1615975 3-1616230 3-1616890 3-1616149 3-1614093 3-1614377 3-1614093 3-1616603 3-1616889 3-609535 3-609841 3-610277 3-609535 3-609841 3-610277 3-609715 3-610140 3-609841 3-609715 3-610277 3-610140 3-609535 3-609368 3-609775 3-610121 3-610389 3-609715 3-610140 3-609715

Quantity Affected: 16,504 cases total

Reason for Recall

Potential Salmonella Contamination

Distribution

Product was distributed to AZ, CA, IL, FL, WI, MA, MS, MN, CA, NC, VA, TN, VT, CT, NY, MD, PA, NJ, TX

Type: Voluntary: Firm initiated

Recall Initiated: 2025-05-20

Company

LIPMAN FAMILY FARMS

Immokalee, FL

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 161 food recalls issued in the same week, part of 204 food-related FDA actions this month.

LIPMAN FAMILY FARMS 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 (LIPMAN FAMILY FARMS) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does LIPMAN FAMILY FARMS have FDA actions?

LIPMAN FAMILY FARMS 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-0026-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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