Fruteria V.I.P.
FDA import alert and refusal historyJuarez, MexicoFEI 3009188801
Recorded by FDA as FRUTERIA V.I.P.
As of October 26, 2026, Fruteria V.I.P. (Juarez, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for key lime; prickley pear; nopales; poblano peppers, published by FDA on September 7, 2011, and has 2 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
- Prickle pear (core fruit) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Fruteria V.I.P.
3 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- PESTICIDE2 refused lines
Pesticide chemical residue
The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that food.
Questions about Fruteria V.I.P.
- Is Fruteria V.I.P. on an FDA import alert?
- Yes. As of October 26, 2026, Fruteria V.I.P. is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for key lime; prickley pear; nopales; poblano peppers; FDA published the listing on September 7, 2011.
- Has FDA refused shipments from Fruteria V.I.P.?
- Yes. FDA refused 2 shipment lines from Fruteria V.I.P. between January 31, 2019 and July 9, 2019. The most recent, on July 9, 2019, was prickle pear (core fruit), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Fruteria V.I.P.'s shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Fruteria V.I.P.'s FEI number?
- Fruteria V.I.P.'s FDA Establishment Identifier (FEI) is 3009188801.
- Can shipments from Fruteria V.I.P. still enter the U.S.?
- Shipments of key lime; prickley pear; nopales; poblano peppers from Fruteria V.I.P. 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.