DULCES VERO, S.A. de C.V.
FDA import alert and refusal historyGuadalajara, MexicoFEI 3004254762
As of October 26, 2026, DULCES VERO, S.A. de C.V. (Guadalajara, Mexico) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for lollipop (without chocolate), 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 DULCES VERO, 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 listLollipop (without Chocolate)Source
Questions about DULCES VERO, S.A. de C.V.
- Is DULCES VERO, S.A. de C.V. on an FDA import alert?
- Yes. As of October 26, 2026, DULCES VERO, S.A. de C.V. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for lollipop (without chocolate); FDA published the listing on September 18, 2009.
- Has FDA refused shipments from DULCES VERO, S.A. de C.V.?
- No FDA import refusals for DULCES VERO, S.A. de C.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is DULCES VERO, S.A. de C.V.'s FEI number?
- DULCES VERO, S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3004254762.
- Can shipments from DULCES VERO, S.A. de C.V. still enter the U.S.?
- Shipments of lollipop (without chocolate) from DULCES VERO, 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).
Buying from DULCES VERO, S.A. de C.V.?
Watch it and get the FDA record the day it changes. Free for one supplier.
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.