Bonita Papaya Spr de RL
FDA import alert and refusal historyTecoman, MexicoFEI 3013670241
Recorded by FDA as BONITA PAPAYA SPR DE RL
As of October 26, 2026, Bonita Papaya 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) · SALMONELLA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Bonita Papaya Spr de RL
2 records, newest first. Each line links to the FDA page it came from.
2023
- Import alert listingListed on Import Alert 21-17green listPapayaSource
2019
- Import refusalRefused, Papaya (papaw) (subtropical and tropical fruit)SALMONELLAEntry BYX-0163166-6Source
Refusal charges, in plain English
- SALMONELLA1 refused line
Salmonella
The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
Questions about Bonita Papaya Spr de RL
- Is Bonita Papaya Spr de RL on an FDA import alert?
- Yes. As of October 26, 2026, Bonita Papaya Spr de RL is on the green list of FDA Import Alert 21-17, “Papaya from Mexico”, for papaya; FDA published the listing on January 19, 2023.
- Has FDA refused shipments from Bonita Papaya Spr de RL?
- Yes. FDA refused 1 shipment line from Bonita Papaya Spr de RL on July 31, 2019. The most recent, on July 31, 2019, was papaya (papaw) (subtropical and tropical fruit), charged as SALMONELLA (salmonella).
- Why did FDA refuse Bonita Papaya Spr de RL's shipments?
- The most frequent charge is SALMONELLA (salmonella, 1 line).
- What is Bonita Papaya Spr de RL's FEI number?
- Bonita Papaya Spr de RL's FDA Establishment Identifier (FEI) is 3013670241.
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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.