Maria Bakers
FDA import alert and refusal historyKottayam District, IndiaFEI 3011053126
Recorded by FDA as MARIA BAKERS
As of October 26, 2026, Maria Bakers (Kottayam District, India) is on the red list of FDA Import Alert 23-14 (Food products: mycotoxins) for frozen roasted peanut, published by FDA on July 7, 2017, and has 2 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 23-14 · red list
- Last import refusal
- Peanut, shelled · AFLATOXIN
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Maria Bakers
3 records, newest first. Each line links to the FDA page it came from.
2018
2017
- Import alert listingListed on Import Alert 23-14red listFrozen Roasted PeanutSource
- Import refusalRefused, Peanut, shelledAFLATOXINNUTRIT LBLEntry 594-0279993-2Source
Refusal charges, in plain English
- AFLATOXIN2 refused lines
AFLATOXIN
- NUTRIT LBL1 refused line
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
Questions about Maria Bakers
- Is Maria Bakers on an FDA import alert?
- Yes. As of October 26, 2026, Maria Bakers is on the red list of FDA Import Alert 23-14, “Food products: mycotoxins”, for frozen roasted peanut; FDA published the listing on July 7, 2017.
- Has FDA refused shipments from Maria Bakers?
- Yes. FDA refused 2 shipment lines from Maria Bakers between May 4, 2017 and December 14, 2018. The most recent, on December 14, 2018, was peanut, shelled, charged as AFLATOXIN (aflatoxin).
- Why did FDA refuse Maria Bakers's shipments?
- The most frequent charges are AFLATOXIN (aflatoxin, 2 lines) and NUTRIT LBL (nutrition information missing from label, 1 line).
- What is Maria Bakers's FEI number?
- Maria Bakers's FDA Establishment Identifier (FEI) is 3011053126.
- Can shipments from Maria Bakers still enter the U.S.?
- Shipments of frozen roasted peanut from Maria Bakers can be detained without physical examination under Import Alert 23-14; 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.