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Abir International

FDA import alert and refusal historyLudhiana, IndiaFEI 3011215054

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Example subjectAbir Internationa added to Import Alert 16-129 (red list)

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As of October 25, 2026, Abir International (Ludhiana, India) is on the red list of FDA Import Alert 99-45 (Foods that are or contain an unsafe food additive) for white musli whole; inder jon kadve, published by FDA on November 18, 2025, is also listed on Import Alert 99-39 (red list), and has 10 FDA import refusals recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Last import refusal
Herbals & botanicals (not teas), n.e.c. · UNSAFE ADD
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Abir International

13 records, newest first. Each line links to the FDA page it came from.

2026

  1. Import refusal
    Refused, 2 lines in one entry: Herbals & botanicals (not teas), n.e.c.UNSAFE ADDNO ENGLISHEntry 8P5-0084156-1Show 2 lines
    Source

2025

  1. Import alert listing
    Listed on Import Alert 99-45red listWhite Musli Whole; Inder Jon Kadve
    Source

2024

  1. Import refusal
    Refused, Herbals & botanicals (not teas), n.e.c.LIST INGRENO ENGLISHUSUAL NAMEEntry 8P5-0051775-7
    Source
  2. Import refusal
    Refused, 6 lines in one entry: Ashwagandha (herbal & botanicals, not teas); Herbals & botanicals (not teas), n.e.c.POISONOUSUSUAL NAMENUTRIT LBLNO ENGLISHEntry 8P5-0039844-8Show 6 lines
    Source
  3. Import alert listing
    Listed on Import Alert 99-39red listWhite Musli Whole; Lodh Powder; Ratan Jot (Ratanjot); Inder Jon Kadve; Nashodar
    Source

2023

  1. Import refusal
    Refused, Other bakery products, n.e.c.FILTHYEntry 8P5-0030660-7
    Source
  2. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

Refusal charges, in plain English

  • NO ENGLISH8 refused lines

    Required label information not in English

    Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

  • USUAL NAME7 refused lines

    Common or usual name missing

    The label appeared not to show the common or usual name of the food.

  • 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.

  • UNSAFE ADD2 refused lines

    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.

  • 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.

  • LIST INGRE1 refused line

    Ingredients not listed

    The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).

  • POISONOUS1 refused line

    Poisonous or deleterious substance

    The product appeared to bear or contain a poisonous or deleterious substance which may render it injurious to health.

Questions about Abir International

Is Abir International on an FDA import alert?
Yes. As of October 25, 2026, Abir International is on the red list of FDA Import Alert 99-45, “Foods that are or contain an unsafe food additive”, for white musli whole; inder jon kadve; FDA published the listing on November 18, 2025.
Has FDA refused shipments from Abir International?
Yes. FDA refused 10 shipment lines from Abir International between April 10, 2023 and January 6, 2026. The most recent, on January 6, 2026, was herbals & botanicals (not teas), n.e.c., charged as UNSAFE ADD (food additive unsafe under section 409).
Why did FDA refuse Abir International's shipments?
The most frequent charges are NO ENGLISH (required label information not in english, 8 lines) and USUAL NAME (common or usual name missing, 7 lines).
When was Abir International last inspected by FDA?
FDA's most recent inspection of Abir International with a final classification is dated January 4, 2023 and was classified VAI (Voluntary Action Indicated).
What is Abir International's FEI number?
Abir International's FDA Establishment Identifier (FEI) is 3011215054.
Can shipments from Abir International still enter the U.S.?
Shipments of white musli whole; inder jon kadve from Abir International can be detained without physical examination under Import Alert 99-45; 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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Example subjectAbir Internationa added to Import Alert 16-129 (red list)

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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.