Usizine Lave Luxe Industrials
FDA import alert and refusal historyBeyrouth, LebanonFEI 3036659823
Recorded by FDA as USIZINE LAVE LUXE INDUSTRIALS
As of October 26, 2026, Usizine Lave Luxe Industrials is not on any FDA import alert in SupplierRadar's records; FDA refused 6 of its shipment lines between April 30, 2025 and July 17, 2026, 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
- Vegetable & vegetable products not mentioned elsewhere, n.e.c. · NO PROCESS
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Usizine Lave Luxe Industrials
6 records, newest first. Each line links to the FDA page it came from.
2026
- Import refusalSource
Refused, 2 lines in one entry: Vegetable & vegetable products not mentioned elsewhere, n.e.c.NO PROCESSEntry 196-2556638-5Show 2 linesHide lines
- Refused, Vegetable & vegetable products not mentioned elsewhere, n.e.c.NO PROCESSEntry 196-2556638-5Source
- Refused, Vegetable & vegetable products not mentioned elsewhere, n.e.c.NO PROCESSEntry 196-2556638-5Source
- Import refusalRefused, Tamarind, topping or syrupFILTHYEntry 196-2559144-1Source
- Import refusalRefused, Vegetable & vegetable products not mentioned elsewhere, n.e.c.NUTRIT LBLNEEDS FCENO PROCESSEntry 196-2559676-2Source
2025
- Import refusalRefused, Vegetable & vegetable products not mentioned elsewhere, n.e.c.NEEDS FCENO PROCESSEntry 196-2555785-5Source
- Import refusalRefused, Olive oil, refined, single ingredientPESTICIDELABELINGNUTRIT LBLEntry 196-2555195-7Source
Refusal charges, in plain English
- NO PROCESS4 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.
- NEEDS FCE2 refused lines
Processor not registered for canned or acidified foods
The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.
- NUTRIT LBL2 refused lines
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
- 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.
- 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 Usizine Lave Luxe Industrials
- Is Usizine Lave Luxe Industrials on an FDA import alert?
- No listing for Usizine Lave Luxe Industrials appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Lebanon page.
- Has FDA refused shipments from Usizine Lave Luxe Industrials?
- Yes. FDA refused 6 shipment lines from Usizine Lave Luxe Industrials between April 30, 2025 and July 17, 2026. The most recent, on July 17, 2026, was vegetable & vegetable products not mentioned elsewhere, n.e.c., charged as NO PROCESS (no scheduled process filed).
- Why did FDA refuse Usizine Lave Luxe Industrials's shipments?
- The most frequent charges are NO PROCESS (no scheduled process filed, 4 lines) and NEEDS FCE (processor not registered for canned or acidified foods, 2 lines).
- What is Usizine Lave Luxe Industrials's FEI number?
- Usizine Lave Luxe Industrials's FDA Establishment Identifier (FEI) is 3036659823.
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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.