Rachidi Group For Trade & Industry
FDA import alert and refusal historyAsh Shuwayfat, LebanonFEI 3014654860
Recorded by FDA as RACHIDI GROUP FOR TRADE & INDUSTRY
As of October 26, 2026, Rachidi Group For Trade & Industry (Ash Shuwayfat, Lebanon) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for dried mallow molokhia (dry jews mallow), published by FDA on June 12, 2024, and has 4 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-08 · red list
- Last import refusal
- Molasses · STD IDENT
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Rachidi Group For Trade & Industry
5 records, newest first. Each line links to the FDA page it came from.
2024
- Import refusalSource
Refused, 2 lines in one entry: Molasses; Waffles without custard or cream fillingSTD IDENTLABELINGEntry K09-0091771-5Show 2 linesHide lines
- Import alert listingListed on Import Alert 99-08red listDRIED MALLOW Molokhia (DRY JEWS MALLOW)Source
- Import refusalSource
2021
- Import refusalRefused, Mixed nuts, shelled, n.e.c.UNSAFE COLUNSAFE ADDLACKS N/CEntry K09-0081628-9Source
Refusal charges, in plain English
- FILTHY1 refused line
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.
- LABELING1 refused line
Fair Packaging and Labeling Act
The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.
- LACKS N/C1 refused line
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.
- 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.
- STD IDENT1 refused line
Does not conform to standard of identity
The product appeared to be represented as a food that has an FDA standard of identity, but not to conform to that standard.
- UNSAFE ADD1 refused line
Food additive unsafe under section 409
The product appeared to contain a food additive that is unsafe within the meaning of section 409 of the FD&C Act, the section that governs which food additives may be used and under what conditions.
- UNSAFE COL1 refused line
Color additive unsafe under section 721
The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.
Questions about Rachidi Group For Trade & Industry
- Is Rachidi Group For Trade & Industry on an FDA import alert?
- Yes. As of October 26, 2026, Rachidi Group For Trade & Industry is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for dried mallow molokhia (dry jews mallow); FDA published the listing on June 12, 2024.
- Has FDA refused shipments from Rachidi Group For Trade & Industry?
- Yes. FDA refused 4 shipment lines from Rachidi Group For Trade & Industry between February 11, 2021 and July 31, 2024. The most recent, on July 31, 2024, was molasses, charged as STD IDENT (does not conform to standard of identity).
- Why did FDA refuse Rachidi Group For Trade & Industry's shipments?
- The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 1 line) and LABELING (fair packaging and labeling act, 1 line).
- What is Rachidi Group For Trade & Industry's FEI number?
- Rachidi Group For Trade & Industry's FDA Establishment Identifier (FEI) is 3014654860.
- Can shipments from Rachidi Group For Trade & Industry still enter the U.S.?
- Shipments of dried mallow molokhia (dry jews mallow) from Rachidi Group For Trade & Industry can be detained without physical examination under Import Alert 99-08; 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.