Prism Farms
FDA import alert and refusal historyLeamington, CanadaFEI 3002851274
As of October 26, 2026, Prism Farms is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines between June 4, 2026 and July 9, 2026, most often for filthy, putrid or decomposed substance (FILTHY).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Cucumbers (fruit used as vegetable) · FILTHY
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Prism Farms
4 records, newest first. Each line links to the FDA page it came from.
2026
2011
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
Refusal charges, in plain English
- FILTHY3 refused lines
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.
Questions about Prism Farms
- Is Prism Farms on an FDA import alert?
- No listing for Prism Farms appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Canada page.
- Has FDA refused shipments from Prism Farms?
- Yes. FDA refused 3 shipment lines from Prism Farms between June 4, 2026 and July 9, 2026. The most recent, on July 9, 2026, was cucumbers (fruit used as vegetable), charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Prism Farms's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 3 lines).
- When was Prism Farms last inspected by FDA?
- FDA's most recent inspection of Prism Farms with a final classification is dated May 16, 2011 and was classified VAI (Voluntary Action Indicated).
- What is Prism Farms's FEI number?
- Prism Farms's FDA Establishment Identifier (FEI) is 3002851274.
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.