Planta HBS Delli, S.A. de C.V.
FDA import alert and refusal historyVilla Uman, MexicoFEI 3010302409
As of October 26, 2026, Planta HBS Delli, S.A. de C.V. (Villa Uman, Mexico) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for beverage base non-fruit liquid; imit flav beverage base liq; comb true imit flav base liq; jamaica hibiscus syrup, published by FDA on September 18, 2009, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 45-02 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Planta HBS Delli, S.A. de C.V.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 45-02red listBeverage Base Non-Fruit Liquid; Imit Flav Beverage Base Liq; Comb True Imit Flav Base Liq; jamaica hibiscus syrupSource
Questions about Planta HBS Delli, S.A. de C.V.
- Is Planta HBS Delli, S.A. de C.V. on an FDA import alert?
- Yes. As of October 26, 2026, Planta HBS Delli, S.A. de C.V. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for beverage base non-fruit liquid; imit flav beverage base liq; comb true imit flav base liq; jamaica hibiscus syrup; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Planta HBS Delli, S.A. de C.V.?
- No FDA import refusals for Planta HBS Delli, S.A. de C.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Planta HBS Delli, S.A. de C.V.'s FEI number?
- Planta HBS Delli, S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3010302409.
- Can shipments from Planta HBS Delli, S.A. de C.V. still enter the U.S.?
- Shipments of beverage base non-fruit liquid; imit flav beverage base liq; comb true imit flav base liq; jamaica hibiscus syrup from Planta HBS Delli, S.A. de C.V. can be detained without physical examination under Import Alert 45-02; 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.