Dona Caro Spr de RL
FDA import alert and refusal historyTecoman, MexicoFEI 3010283607
Recorded by FDA as DONA CARO SPR DE RL
As of October 26, 2026, Dona Caro Spr de RL is on the green list of FDA Import Alert 21-17, which exempts its listed products from detention without physical examination under that alert, 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 21-17 · green list
- Last import refusal
- Papaya (papaw) (subtropical and tropical fruit) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Dona Caro Spr de RL
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 Dona Caro Spr de RL
- Is Dona Caro Spr de RL on an FDA import alert?
- Yes. As of October 26, 2026, Dona Caro Spr de RL is on the green list of FDA Import Alert 21-17, “Papaya from Mexico”, for papaya; FDA published the listing on November 8, 2013.
- Has FDA refused shipments from Dona Caro Spr de RL?
- Yes. FDA refused 2 shipment lines from Dona Caro Spr de RL between April 26, 2017 and September 20, 2019. The most recent, on September 20, 2019, was papaya (papaw) (subtropical and tropical fruit), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Dona Caro Spr de RL's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Dona Caro Spr de RL's FEI number?
- Dona Caro Spr de RL's FDA Establishment Identifier (FEI) is 3010283607.
Buying from Dona Caro Spr de RL?
Watch it and get the FDA record the day it changes. Free for one supplier.
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.