Paul's Greenhouse
FDA import alert and refusal historyOsoyoos, CanadaFEI 3009447520
As of October 26, 2026, Paul's Greenhouse (Osoyoos, Canada) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for cucumbers, published by FDA on June 9, 2016, 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
- Cucumbers (fruit used as vegetable) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Paul's Greenhouse
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 Paul's Greenhouse
- Is Paul's Greenhouse on an FDA import alert?
- Yes. As of October 26, 2026, Paul's Greenhouse is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for cucumbers; FDA published the listing on June 9, 2016.
- Has FDA refused shipments from Paul's Greenhouse?
- Yes. FDA refused 2 shipment lines from Paul's Greenhouse between May 24, 2017 and June 4, 2018. The most recent, on June 4, 2018, was cucumbers (fruit used as vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Paul's Greenhouse's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Paul's Greenhouse's FEI number?
- Paul's Greenhouse's FDA Establishment Identifier (FEI) is 3009447520.
- Can shipments from Paul's Greenhouse still enter the U.S.?
- Shipments of cucumbers from Paul's Greenhouse 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.