Rubio de B.C., S.A. de C.V.
FDA import alert and refusal historyMexicali, MexicoFEI 3004723973
Recorded by FDA as RUBIO DE B.C., S.A. DE C.V.
As of October 26, 2026, Rubio de B.C., S.A. de C.V. (Mexicali, Mexico) is on the red list of FDA Import Alert 41-03 (Adulterated and Misbranded Medical Foods) for electrolit coconut; electrolit apple; electrolit grapefruit; electrolit strawberry; electrolit peach, published by FDA on April 18, 2014, 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 41-03 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Rubio de B.C., S.A. de C.V.
1 record, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 41-03red listElectrolit Coconut; Electrolit Apple; Electrolit Grapefruit; Electrolit Strawberry; Electrolit PeachSource
Questions about Rubio de B.C., S.A. de C.V.
- Is Rubio de B.C., S.A. de C.V. on an FDA import alert?
- Yes. As of October 26, 2026, Rubio de B.C., S.A. de C.V. is on the red list of FDA Import Alert 41-03, “Adulterated and Misbranded Medical Foods”, for electrolit coconut; electrolit apple; electrolit grapefruit; electrolit strawberry; electrolit peach; FDA published the listing on April 18, 2014.
- Has FDA refused shipments from Rubio de B.C., S.A. de C.V.?
- No FDA import refusals for Rubio de B.C., S.A. de C.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Rubio de B.C., S.A. de C.V.'s FEI number?
- Rubio de B.C., S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3004723973.
- Can shipments from Rubio de B.C., S.A. de C.V. still enter the U.S.?
- Shipments of electrolit coconut; electrolit apple; electrolit grapefruit; electrolit strawberry; electrolit peach from Rubio de B.C., S.A. de C.V. can be detained without physical examination under Import Alert 41-03; 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.