RecallRadar
FDA · FoodClass I

pennrose farms LLC food recall: Cucumbers Pennrose Farms

SalmonellaMicrobial contamination

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Terminated
Event ID
96938
Recall initiated
May 20, 2025
Classified by FDA
Jun 3, 2025
Posted in Enforcement Report
Jun 11, 2025
Terminated
Jul 21, 2025
Recalling firm
pennrose farms LLC
Firm location
Wellington, FL, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Products in this event
1

What to do

Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.

View the official FDA record ↗

Reason for recall

Due to potential Salmonella Contamination

What the classification means

  • Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.

About this recall

The firm started this recall on May 20, 2025. FDA classified it 14 days later, on Jun 3, 2025. Distribution reported by FDA: Product was shipped to FL, NJ, GA, IL, OH

Recalled products (1)

  • H-0006-2025 Class I Terminated

    Cucumbers Pennrose Farms, Net Wt. 5lbs(2.26kg) Mesh bag, Distributed by PennRose Farms, LLC Welington, FL 33414, UPC code 841214101714

    Codes / lots: Lot: 48-122, 48-123, 48-124, 48-125 best by date: 5/12/24 packaged between May 2-May 5

    Quantity: 1,152 cases or 9,216 individual units (bags)

Source and freshness

Source
U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
Official notice
FDA Enforcement Report, event 96938
Raw record
openFDA API (JSON)
Dataset last updated by FDA
Nov 3, 2026
Imported by RecallRadar
Nov 4, 2026

Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.