Grupo Gielpeh Spr de Ri
FDA import alert and refusal historyQuecholac, MexicoFEI 3010241163
Recorded by FDA as GRUPO GIELPEH SPR DE RI
As of October 26, 2026, Grupo Gielpeh Spr de Ri (Quecholac, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for celery, published by FDA on November 16, 2021, is also listed on Import Alert 24-23 (green list), and has 6 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 24-23 · green listIA 99-05 · red list
- Last import refusal
- Celery (leaf & stem vegetable) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Grupo Gielpeh Spr de Ri
8 records, newest first. Each line links to the FDA page it came from.
2024
- Import refusalRefused, Celery (leaf & stem vegetable)PESTICIDEEntry HP7-0495831-0Source
- Import alert listingListed on Import Alert 24-23green listCilantroSource
2021
- Import alert listingListed on Import Alert 99-05red listCelerySource
- Import refusalRefused, Celery (leaf & stem vegetable)PESTICIDEEntry HP7-0442227-5Source
2017
- Import refusalSource
Refused, 3 lines in one entry: Scallions, green onions (root & tuber vegetable); Squash, summer (fruit used as vegetable) and 1 moreLACKS FIRMLACKS N/CUSUAL NAMEEntry BJG-0046189-6Show 3 linesHide lines
- Refused, Scallions, green onions (root & tuber vegetable)LACKS FIRMLACKS N/CUSUAL NAMEEntry BJG-0046189-6Source
- Refused, Squash, summer (fruit used as vegetable)LACKS FIRMLACKS N/CUSUAL NAMEEntry BJG-0046189-6Source
- Refused, Pepper, hot, n.e.c. (fruit used as vegetable)LACKS FIRMLACKS N/CUSUAL NAMEEntry BJG-0046189-6Source
- Import refusalRefused, Cilantro (leaf & stem vegetable)LACKS FIRMLACKS N/CUSUAL NAMEEntry BJG-0046189-6Source
Refusal charges, in plain English
- LACKS FIRM4 refused lines
Manufacturer name and address missing
The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.
- LACKS N/C4 refused lines
Net quantity statement missing
The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.
- USUAL NAME4 refused lines
Common or usual name missing
The label appeared not to show the common or usual name of the food.
- 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 Grupo Gielpeh Spr de Ri
- Is Grupo Gielpeh Spr de Ri on an FDA import alert?
- Yes. As of October 26, 2026, Grupo Gielpeh Spr de Ri is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for celery; FDA published the listing on November 16, 2021.
- Has FDA refused shipments from Grupo Gielpeh Spr de Ri?
- Yes. FDA refused 6 shipment lines from Grupo Gielpeh Spr de Ri between March 1, 2017 and June 5, 2024. The most recent, on June 5, 2024, was celery (leaf & stem vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Grupo Gielpeh Spr de Ri's shipments?
- The most frequent charges are LACKS FIRM (manufacturer name and address missing, 4 lines) and LACKS N/C (net quantity statement missing, 4 lines).
- What is Grupo Gielpeh Spr de Ri's FEI number?
- Grupo Gielpeh Spr de Ri's FDA Establishment Identifier (FEI) is 3010241163.
- Can shipments from Grupo Gielpeh Spr de Ri still enter the U.S.?
- Shipments of celery from Grupo Gielpeh Spr de Ri 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.