H&C Global Supplies SA de CV
FDA import alert and refusal historyTlajomulco De Zuniga, MexicoFEI 2000029737
Recorded by FDA as H&C GLOBAL SUPPLIES SA DE CV
As of October 26, 2026, H&C Global Supplies SA de CV (Tlajomulco De Zuniga, Mexico) is on the red list of FDA Import Alert 99-23 (Produce: contamination with human pathogens) for papaya, published by FDA on August 1, 2011, is also listed on Import Alert 99-05 (red list), 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 listIA 99-05 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for H&C Global Supplies SA de CV
2 records, newest first. Each line links to the FDA page it came from.
2011
- Import alert listingListed on Import Alert 99-23red listPapayaSource
- Import alert listingListed on Import Alert 99-05red listPapayaSource
Questions about H&C Global Supplies SA de CV
- Is H&C Global Supplies SA de CV on an FDA import alert?
- Yes. As of October 26, 2026, H&C Global Supplies SA de CV is on the red list of FDA Import Alert 99-23, “Produce: contamination with human pathogens”, for papaya; FDA published the listing on August 1, 2011.
- Has FDA refused shipments from H&C Global Supplies SA de CV?
- No FDA import refusals for H&C Global Supplies SA de CV appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is H&C Global Supplies SA de CV's FEI number?
- H&C Global Supplies SA de CV's FDA Establishment Identifier (FEI) is 2000029737.
- Can shipments from H&C Global Supplies SA de CV still enter the U.S.?
- Shipments of papaya from H&C Global Supplies SA de CV 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).
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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.