Ng Groupjc SA de CV
FDA import alert and refusal historyMonterrey, MexicoFEI 3012274504
Recorded by FDA as NG GROUPJC SA DE CV
As of October 26, 2026, Ng Groupjc SA de CV (Monterrey, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for habanero peppers, published by FDA on November 29, 2016, and has 2 FDA import refusals 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
- Pepper, hot, n.e.c. (fruit used as vegetable) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Ng Groupjc SA de CV
3 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- PESTICIDE2 refused lines
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 Ng Groupjc SA de CV
- Is Ng Groupjc SA de CV on an FDA import alert?
- Yes. As of October 26, 2026, Ng Groupjc SA de CV is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for habanero peppers; FDA published the listing on November 29, 2016.
- Has FDA refused shipments from Ng Groupjc SA de CV?
- Yes. FDA refused 2 shipment lines from Ng Groupjc SA de CV between October 27, 2016 and August 7, 2018. The most recent, on August 7, 2018, was pepper, hot, n.e.c. (fruit used as vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Ng Groupjc SA de CV's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Ng Groupjc SA de CV's FEI number?
- Ng Groupjc SA de CV's FDA Establishment Identifier (FEI) is 3012274504.
- Can shipments from Ng Groupjc SA de CV still enter the U.S.?
- Shipments of habanero peppers from Ng Groupjc SA de CV 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.