Grupo Alinorsa
FDA import alert and refusal historyMonterrey, MexicoFEI 3011844545
As of October 25, 2026, Grupo Alinorsa is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines between April 4, 2017 and September 24, 2018, most often for no scheduled process filed (NO PROCESS).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Pepper sauce (hot, mild, etc.) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Grupo Alinorsa
3 records, newest first. Each line links to the FDA page it came from.
2018
2017
- Import refusalSource
Refused, 2 lines in one entry: SalsaNO PROCESSEntry WJL-0050785-4Show 2 linesHide lines
- Refused, SalsaNO PROCESSEntry WJL-0050785-4Source
- Refused, SalsaNO PROCESSEntry WJL-0050785-4Source
Refusal charges, in plain English
- NO PROCESS2 refused lines
No scheduled process filed
The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.
- 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 Grupo Alinorsa
- Is Grupo Alinorsa on an FDA import alert?
- No listing for Grupo Alinorsa appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Mexico page.
- Has FDA refused shipments from Grupo Alinorsa?
- Yes. FDA refused 3 shipment lines from Grupo Alinorsa between April 4, 2017 and September 24, 2018. The most recent, on September 24, 2018, was pepper sauce (hot, mild, etc.), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Grupo Alinorsa's shipments?
- The most frequent charges are NO PROCESS (no scheduled process filed, 2 lines) and PESTICIDE (pesticide chemical residue, 1 line).
- What is Grupo Alinorsa's FEI number?
- Grupo Alinorsa's FDA Establishment Identifier (FEI) is 3011844545.
Buying from Grupo Alinorsa?
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.