Marley Farms
FDA import alert and refusal historyTeeswater, CanadaFEI 3009946031
As of October 26, 2026, Marley Farms (Teeswater, Canada) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for mixed hay (timothy hay; alfalfa hay; orchard grass), published by FDA on April 25, 2025, and has 2 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-05 · red list
- Last import refusal
- Grain straw hay · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Marley Farms
3 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- PESTICIDE2 refused lines
Pesticide chemical residue
The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that food.
Questions about Marley Farms
- Is Marley Farms on an FDA import alert?
- Yes. As of October 26, 2026, Marley Farms is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for mixed hay (timothy hay; alfalfa hay; orchard grass); FDA published the listing on April 25, 2025.
- Has FDA refused shipments from Marley Farms?
- Yes. FDA refused 2 shipment lines from Marley Farms between April 16, 2025 and May 22, 2025. The most recent, on May 22, 2025, was grain straw hay, charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Marley Farms's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Marley Farms's FEI number?
- Marley Farms's FDA Establishment Identifier (FEI) is 3009946031.
- Can shipments from Marley Farms still enter the U.S.?
- Shipments of mixed hay (timothy hay; alfalfa hay; orchard grass) from Marley Farms can be detained without physical examination under Import Alert 99-05; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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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.