Agro Source Ltd
FDA import alert and refusal historyDawson Creek, CanadaFEI 3011068289
As of October 26, 2026, Agro Source Ltd (Dawson Creek, Canada) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for red lentils; feed, published by FDA on November 25, 2024, 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 99-08 · red list
- Last import refusal
- Byprod for animal, n.e.c. · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Agro Source Ltd
2 records, newest first. Each line links to the FDA page it came from.
2024
- Import alert listingListed on Import Alert 99-08red listRed Lentils; FeedSource
2018
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 Agro Source Ltd
- Is Agro Source Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Agro Source Ltd is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for red lentils; feed; FDA published the listing on November 25, 2024.
- Has FDA refused shipments from Agro Source Ltd?
- Yes. FDA refused 1 shipment line from Agro Source Ltd on June 22, 2018. The most recent, on June 22, 2018, was byprod for animal, n.e.c., charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Agro Source Ltd's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 1 line).
- What is Agro Source Ltd's FEI number?
- Agro Source Ltd's FDA Establishment Identifier (FEI) is 3011068289.
- Can shipments from Agro Source Ltd still enter the U.S.?
- Shipments of red lentils; feed from Agro Source Ltd can be detained without physical examination under Import Alert 99-08; 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.