Pallodino Export
FDA import alert and refusal historyHighgate, JamaicaFEI 3004812151
As of October 25, 2026, Pallodino Export (Highgate, Jamaica) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for papaya, published by FDA on June 8, 2012, 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 99-05 · red 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 Pallodino Export
2 records, newest first. Each line links to the FDA page it came from.
2017
2012
- Import alert listingListed on Import Alert 99-05red 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 Pallodino Export
- Is Pallodino Export on an FDA import alert?
- Yes. As of October 25, 2026, Pallodino Export is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for papaya; FDA published the listing on June 8, 2012.
- Has FDA refused shipments from Pallodino Export?
- Yes. FDA refused 1 shipment line from Pallodino Export on July 6, 2017. The most recent, on July 6, 2017, was papaya (papaw) (subtropical and tropical fruit), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Pallodino Export's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 1 line).
- What is Pallodino Export's FEI number?
- Pallodino Export's FDA Establishment Identifier (FEI) is 3004812151.
- Can shipments from Pallodino Export still enter the U.S.?
- Shipments of papaya from Pallodino Export 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.