RecallRadar
FDA · FoodClass I

Piazza Produce (dba CIBUS Fresh) food recall: Cibus Fresh

Microbial contamination

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Terminated
Event ID
99470
Recall initiated
Jul 20, 2026
Classified by FDA
Aug 27, 2026
Posted in Enforcement Report
Aug 19, 2026
Terminated
Sep 10, 2026
Recalling firm
Piazza Produce (dba CIBUS Fresh)
Firm location
Noblesville, IN, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
Telephone
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

Possible Cyclospora 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 Jul 20, 2026. FDA classified it 38 days later, on Aug 27, 2026. Distribution reported by FDA: Illinois, Indiana, Kentucky, Mississippi, Ohio and Tennessee Piazza Produce (dba CIBUS Fresh) has 2 recalls in our records.

Recalled products (1)

  • H-1300-2026 Class I Terminated

    Cibus Fresh, Sprig & Sprout, and Jack & Olive brand Garden Salad, 7.75oz clear plastic container, UPC 810028250253

    Codes / lots: Best by/Enjoy by dates: 7/13/2026, 7/14/2026/, 7/16/2026, 7/17/2026, 7/18/2026, 7/19/2026, 7/20/2026

    Quantity: 1279 retail units

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 99470
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.