Fruteria Rerm SA de CV
FDA import alert and refusal historyJuarez, MexicoFEI 3015107662
Recorded by FDA as FRUTERIA RERM SA DE CV
As of October 26, 2026, Fruteria Rerm SA de CV (Juarez, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for fresh watermelons, published by FDA on March 25, 2015, and has 3 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
- Watermelon (vine fruit) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Fruteria Rerm SA de CV
4 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- PESTICIDE3 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 Rerm SA de CV
- Is Fruteria Rerm SA de CV on an FDA import alert?
- Yes. As of October 26, 2026, Fruteria Rerm SA de CV is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for fresh watermelons; FDA published the listing on March 25, 2015.
- Has FDA refused shipments from Fruteria Rerm SA de CV?
- Yes. FDA refused 3 shipment lines from Fruteria Rerm SA de CV between March 2, 2017 and April 6, 2023. The most recent, on April 6, 2023, was watermelon (vine fruit), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Fruteria Rerm SA de CV's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 3 lines).
- What is Fruteria Rerm SA de CV's FEI number?
- Fruteria Rerm SA de CV's FDA Establishment Identifier (FEI) is 3015107662.
- Can shipments from Fruteria Rerm SA de CV still enter the U.S.?
- Shipments of fresh watermelons from Fruteria Rerm SA de CV 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.