Coocastel
FDA import alert and refusal historySao Jose Dos Pinhais, BrazilFEI 3015390983
Recorded by FDA as COOCASTEL
As of October 26, 2026, Coocastel (Sao Jose Dos Pinhais, Brazil) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for banana flour, published by FDA on December 13, 2019, 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 99-39 · red list
- Last import refusal
- Flours and meals n.e.c. · POISONOUS
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Coocastel
2 records, newest first. Each line links to the FDA page it came from.
2019
- Import alert listingListed on Import Alert 99-39red listBanana flourSource
- Import refusalRefused, Flours and meals n.e.c.POISONOUSEntry EGS-5033351-5Source
Refusal charges, in plain English
- 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 Coocastel
- Is Coocastel on an FDA import alert?
- Yes. As of October 26, 2026, Coocastel is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for banana flour; FDA published the listing on December 13, 2019.
- Has FDA refused shipments from Coocastel?
- Yes. FDA refused 1 shipment line from Coocastel on September 6, 2019. The most recent, on September 6, 2019, was flours and meals n.e.c., charged as POISONOUS (poisonous or deleterious substance).
- Why did FDA refuse Coocastel's shipments?
- The most frequent charge is POISONOUS (poisonous or deleterious substance, 1 line).
- What is Coocastel's FEI number?
- Coocastel's FDA Establishment Identifier (FEI) is 3015390983.
- Can shipments from Coocastel still enter the U.S.?
- Shipments of banana flour from Coocastel can be detained without physical examination under Import Alert 99-39; 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.