Consorcio Hermanos Suriel Acosta
FDA import alert and refusal historyPadre Fantino, Dominican RepublicFEI 3008300613
As of October 26, 2026, Consorcio Hermanos Suriel Acosta (Padre Fantino, Dominican Republic) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for cinnamon lollipops; milk and orange lollipops; fruit punch lollipops; coconut pineapple lollipops, published by FDA on November 5, 2010, 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 Consorcio Hermanos Suriel Acosta
1 record, newest first. Each line links to the FDA page it came from.
2010
- Import alert listingListed on Import Alert 45-02red listCinnamon Lollipops; Milk and Orange Lollipops; Fruit Punch Lollipops; Coconut Pineapple LollipopsSource
Questions about Consorcio Hermanos Suriel Acosta
- Is Consorcio Hermanos Suriel Acosta on an FDA import alert?
- Yes. As of October 26, 2026, Consorcio Hermanos Suriel Acosta is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for cinnamon lollipops; milk and orange lollipops; fruit punch lollipops; coconut pineapple lollipops; FDA published the listing on November 5, 2010.
- Has FDA refused shipments from Consorcio Hermanos Suriel Acosta?
- No FDA import refusals for Consorcio Hermanos Suriel Acosta appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Consorcio Hermanos Suriel Acosta's FEI number?
- Consorcio Hermanos Suriel Acosta's FDA Establishment Identifier (FEI) is 3008300613.
- Can shipments from Consorcio Hermanos Suriel Acosta still enter the U.S.?
- Shipments of cinnamon lollipops; milk and orange lollipops; fruit punch lollipops; coconut pineapple lollipops from Consorcio Hermanos Suriel Acosta 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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