Herbafood SA de CV
FDA import alert and refusal historyTlaquepaque, MexicoFEI 3019983330
Recorded by FDA as HERBAFOOD SA DE CV
As of October 26, 2026, Herbafood SA de CV (Tlaquepaque, Mexico) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for winter shot powder with ginger; echinacea and tibet mushroom (code 3373), published by FDA on October 17, 2024, 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
- Vitamin, n.e.c. · BACTERIA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Herbafood SA de CV
2 records, newest first. Each line links to the FDA page it came from.
2024
- Import alert listingListed on Import Alert 99-39red listWinter Shot Powder with Ginger; Echinacea and Tibet Mushroom (Code 3373)Source
2022
- Import refusalSource
Refusal charges, in plain English
Questions about Herbafood SA de CV
- Is Herbafood SA de CV on an FDA import alert?
- Yes. As of October 26, 2026, Herbafood SA de CV is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for winter shot powder with ginger; echinacea and tibet mushroom (code 3373); FDA published the listing on October 17, 2024.
- Has FDA refused shipments from Herbafood SA de CV?
- Yes. FDA refused 1 shipment line from Herbafood SA de CV on July 29, 2022. The most recent, on July 29, 2022, was vitamin, n.e.c., charged as BACTERIA (bacteria).
- Why did FDA refuse Herbafood SA de CV's shipments?
- The most frequent charges are BACTERIA (bacteria, 1 line) and SUPPL GMP (dietary supplement cgmp not met, 1 line).
- What is Herbafood SA de CV's FEI number?
- Herbafood SA de CV's FDA Establishment Identifier (FEI) is 3019983330.
- Can shipments from Herbafood SA de CV still enter the U.S.?
- Shipments of winter shot powder with ginger; echinacea and tibet mushroom (code 3373) from Herbafood SA de CV 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.