Marhaven Agri
FDA import alert and refusal historyAlma, CanadaFEI 2000030435
As of October 26, 2026, Marhaven Agri (Alma, Canada) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for blueberries, published by FDA on May 23, 2025, and has 1 FDA import refusal 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
- Mixed hay · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Marhaven Agri
2 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalRefused, Mixed hayPESTICIDEEntry 572-6903423-7Source
- Import alert listingListed on Import Alert 99-05red listBlueberriesSource
Refusal charges, in plain English
- PESTICIDE1 refused line
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 Marhaven Agri
- Is Marhaven Agri on an FDA import alert?
- Yes. As of October 26, 2026, Marhaven Agri is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for blueberries; FDA published the listing on May 23, 2025.
- Has FDA refused shipments from Marhaven Agri?
- Yes. FDA refused 1 shipment line from Marhaven Agri on June 12, 2025. The most recent, on June 12, 2025, was mixed hay, charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Marhaven Agri's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 1 line).
- What is Marhaven Agri's FEI number?
- Marhaven Agri's FDA Establishment Identifier (FEI) is 2000030435.
- Can shipments from Marhaven Agri still enter the U.S.?
- Shipments of blueberries from Marhaven Agri 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.