Mac Impex
FDA import alert and refusal historyNavi Mumbai, IndiaFEI 3009131985
Recorded by FDA as MAC IMPEX
As of October 26, 2026, Mac Impex (Navi Mumbai, India) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for moong dal (moong bean split), published by FDA on January 17, 2025, is also listed on Import Alert 45-02 (red list), and has 11 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 listIA 45-02 · red list
- Last import refusal
- Mung bean, dried or paste · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Mac Impex
13 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalSource
Refused, 2 lines in one entry: Mung bean, dried or pastePESTICIDEEntry KM6-3645190-8Show 2 linesHide lines
- Import refusalSource
Refused, 3 lines in one entry: Mung bean, dried or pastePESTICIDEEntry KM6-3646795-3Show 3 linesHide lines
- Import alert listingListed on Import Alert 99-08red listMoong Dal (Moong Bean Split)Source
- Import refusalSource
Refused, 2 lines in one entry: Mung bean, dried or pastePESTICIDEEntry KM6-1621837-6Show 2 linesHide lines
2024
- Import refusalRefused, Pepper, black, ground, cracked (spice)FILTHYSALMONELLAEntry KM6-3626714-8Source
2023
2022
- Import alert listingListed on Import Alert 45-02red listFryums/Far-Far starch based product (All Shapes/colors; Number; Pipe; Square and Star)Source
2021
- Import refusalRefused, Other bakery products, n.e.c.UNSAFE COLCOLOR LBLGYELLOW #5Entry 8P5-0009877-4Source
Refusal charges, in plain English
- PESTICIDE7 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.
- FILTHY3 refused lines
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.
- COLOR LBLG1 refused line
Artificial coloring not declared
The product appeared to contain an artificial coloring without labeling that states that fact.
- SALMONELLA1 refused line
Salmonella
The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
- 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.
- YELLOW #51 refused line
FD&C Yellow No. 5 not declared
The food appeared to contain the color additive FD&C Yellow No. 5 without declaring it on the label as 21 CFR 74.705 requires.
Questions about Mac Impex
- Is Mac Impex on an FDA import alert?
- Yes. As of October 26, 2026, Mac Impex is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for moong dal (moong bean split); FDA published the listing on January 17, 2025.
- Has FDA refused shipments from Mac Impex?
- Yes. FDA refused 11 shipment lines from Mac Impex between October 5, 2021 and June 2, 2025. The most recent, on June 2, 2025, was mung bean, dried or paste, charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Mac Impex's shipments?
- The most frequent charges are PESTICIDE (pesticide chemical residue, 7 lines) and FILTHY (filthy, putrid or decomposed substance, 3 lines).
- What is Mac Impex's FEI number?
- Mac Impex's FDA Establishment Identifier (FEI) is 3009131985.
- Can shipments from Mac Impex still enter the U.S.?
- Shipments of moong dal (moong bean split) from Mac Impex 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.