Madon Pure Foods Pvt Lt
FDA import alert and refusal historyMumbai, IndiaFEI 3016610546
Recorded by FDA as MADON PURE FOODS PVT LT
As of October 26, 2026, Madon Pure Foods Pvt Lt (Mumbai, India) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for ground ginger, published by FDA on August 3, 2022, and has 1 FDA import refusal recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-19 · red list
- Last import refusal
- Ginger root, dried or paste · SALMONELLA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Madon Pure Foods Pvt Lt
2 records, newest first. Each line links to the FDA page it came from.
2022
- Import refusalRefused, Ginger root, dried or pasteSALMONELLAEntry 9LB-0002622-2Source
- Import alert listingListed on Import Alert 99-19red listGround GingerSource
Refusal charges, in plain English
- 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.
Questions about Madon Pure Foods Pvt Lt
- Is Madon Pure Foods Pvt Lt on an FDA import alert?
- Yes. As of October 26, 2026, Madon Pure Foods Pvt Lt is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for ground ginger; FDA published the listing on August 3, 2022.
- Has FDA refused shipments from Madon Pure Foods Pvt Lt?
- Yes. FDA refused 1 shipment line from Madon Pure Foods Pvt Lt on August 4, 2022. The most recent, on August 4, 2022, was ginger root, dried or paste, charged as SALMONELLA (salmonella).
- Why did FDA refuse Madon Pure Foods Pvt Lt's shipments?
- The most frequent charge is SALMONELLA (salmonella, 1 line).
- What is Madon Pure Foods Pvt Lt's FEI number?
- Madon Pure Foods Pvt Lt's FDA Establishment Identifier (FEI) is 3016610546.
- Can shipments from Madon Pure Foods Pvt Lt still enter the U.S.?
- Shipments of ground ginger from Madon Pure Foods Pvt Lt can be detained without physical examination under Import Alert 99-19; 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.