Frutioro Mexico Spr de RL
FDA import alert and refusal historyColima, MexicoFEI 3009741480
Recorded by FDA as FRUTIORO MEXICO SPR DE RL
As of October 26, 2026, Frutioro Mexico 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 1 FDA import refusal 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 Frutioro Mexico Spr de RL
2 records, newest first. Each line links to the FDA page it came from.
2024
2013
- Import alert listingListed on Import Alert 21-17green listPapayaSource
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 Frutioro Mexico Spr de RL
- Is Frutioro Mexico Spr de RL on an FDA import alert?
- Yes. As of October 26, 2026, Frutioro Mexico Spr de RL is on the green list of FDA Import Alert 21-17, “Papaya from Mexico”, for papaya; FDA published the listing on April 3, 2013.
- Has FDA refused shipments from Frutioro Mexico Spr de RL?
- Yes. FDA refused 1 shipment line from Frutioro Mexico Spr de RL on November 14, 2024. The most recent, on November 14, 2024, was papaya (papaw) (subtropical and tropical fruit), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Frutioro Mexico Spr de RL's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 1 line).
- What is Frutioro Mexico Spr de RL's FEI number?
- Frutioro Mexico Spr de RL's FDA Establishment Identifier (FEI) is 3009741480.
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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.