Ordorica Produce S.P.R. De R.L.
FDA import alert and refusal historyLa Paz, MexicoFEI 3002615615
As of October 26, 2026, Ordorica Produce S.P.R. De R.L. (La Paz, Mexico) is on the red list of FDA Import Alert 99-23 (Produce: contamination with human pathogens) for papaya, published by FDA on August 8, 2011, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-23 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Ordorica Produce S.P.R. De R.L.
1 record, newest first. Each line links to the FDA page it came from.
2011
- Import alert listingListed on Import Alert 99-23red listPapayaSource
Questions about Ordorica Produce S.P.R. De R.L.
- Is Ordorica Produce S.P.R. De R.L. on an FDA import alert?
- Yes. As of October 26, 2026, Ordorica Produce S.P.R. De R.L. is on the red list of FDA Import Alert 99-23, “Produce: contamination with human pathogens”, for papaya; FDA published the listing on August 8, 2011.
- Has FDA refused shipments from Ordorica Produce S.P.R. De R.L.?
- No FDA import refusals for Ordorica Produce S.P.R. De R.L. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Ordorica Produce S.P.R. De R.L.'s FEI number?
- Ordorica Produce S.P.R. De R.L.'s FDA Establishment Identifier (FEI) is 3002615615.
- Can shipments from Ordorica Produce S.P.R. De R.L. still enter the U.S.?
- Shipments of papaya from Ordorica Produce S.P.R. De R.L. can be detained without physical examination under Import Alert 99-23; 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).
Buying from Ordorica Produce S.P.R. De R.L.?
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.