Montalvos International Produce Of Mexico
FDA import alert and refusal historySan Nicolas De Los Garza, MexicoFEI 3001379983
As of October 26, 2026, Montalvos International Produce Of Mexico (San Nicolas De Los Garza, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for cactus pads, published by FDA on June 14, 2018, 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 99-05 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Montalvos International Produce Of Mexico
1 record, newest first. Each line links to the FDA page it came from.
2018
- Import alert listingListed on Import Alert 99-05red listCactus PadsSource
Questions about Montalvos International Produce Of Mexico
- Is Montalvos International Produce Of Mexico on an FDA import alert?
- Yes. As of October 26, 2026, Montalvos International Produce Of Mexico is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for cactus pads; FDA published the listing on June 14, 2018.
- Has FDA refused shipments from Montalvos International Produce Of Mexico?
- No FDA import refusals for Montalvos International Produce Of Mexico appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Montalvos International Produce Of Mexico's FEI number?
- Montalvos International Produce Of Mexico's FDA Establishment Identifier (FEI) is 3001379983.
- Can shipments from Montalvos International Produce Of Mexico still enter the U.S.?
- Shipments of cactus pads from Montalvos International Produce Of Mexico can be detained without physical examination under Import Alert 99-05; 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.