Cibus Fresh, Sprig & Sprout, and Jack & Olive brand Garden Salad, 7.75oz clear plastic container, UPC 810028250253
Summary
The FDA issued a Class I for Cibus Fresh, Sprig & Sprout, and Jack & Olive brand Garden Salad, 7.75oz clear p by Piazza Produce (dba CIBUS Fresh). Reason: Possible Cyclospora Contamination.
Details
Source
Food Recall
External ID
H-1300-2026
Action Date
2026-08-19
Status
Terminated
Category
food
Product Description
Cibus Fresh, Sprig & Sprout, and Jack & Olive brand Garden Salad, 7.75oz clear plastic container, UPC 810028250253
Lot/Code Info: 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 Affected: 1279 retail units
Reason for Recall
Possible Cyclospora Contamination
Distribution
Illinois, Indiana, Kentucky, Mississippi, Ohio and Tennessee
Type: Voluntary: Firm initiated
Recall Initiated: 2026-07-20
Company
Noblesville, IN
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 63 food recalls issued in the same week, part of 82 food-related FDA actions this month.
Piazza Produce (dba CIBUS Fresh) has 2 FDA actions in our database, including 2 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 (Piazza Produce (dba CIBUS Fresh)) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Piazza Produce (dba CIBUS Fresh) have FDA actions?
Piazza Produce (dba CIBUS Fresh) has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-1300-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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