Adriana Ruz Perry
FDA import alert and refusal historyRequinoa, ChileFEI 3012162300
As of October 26, 2026, Adriana Ruz Perry is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between March 8, 2019 and March 20, 2019, most often for pesticide chemical residue (PESTICIDE).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Nectarine (pit fruit) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Adriana Ruz Perry
2 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.
- LISTERIA1 refused line
Listeria monocytogenes
The product appeared to contain Listeria monocytogenes, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
Questions about Adriana Ruz Perry
- Is Adriana Ruz Perry on an FDA import alert?
- No listing for Adriana Ruz Perry appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Chile page.
- Has FDA refused shipments from Adriana Ruz Perry?
- Yes. FDA refused 2 shipment lines from Adriana Ruz Perry between March 8, 2019 and March 20, 2019. The most recent, on March 20, 2019, was nectarine (pit fruit), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Adriana Ruz Perry's shipments?
- The most frequent charges are PESTICIDE (pesticide chemical residue, 2 lines) and LISTERIA (listeria monocytogenes, 1 line).
- What is Adriana Ruz Perry's FEI number?
- Adriana Ruz Perry's FDA Establishment Identifier (FEI) is 3012162300.
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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.