Mas-Pex
FDA import alert and refusal historyWadowice, PolandFEI 3014018069
Recorded by FDA as MAS-PEX
As of October 26, 2026, Mas-Pex (Wadowice, Poland) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for orange juice, published by FDA on June 7, 2012, and has 1 FDA import refusal recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-08 · red list
- Last import refusal
- Orange, citrus fruit juices or concentrates · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Mas-Pex
2 records, newest first. Each line links to the FDA page it came from.
2024
2012
- Import alert listingListed on Import Alert 99-08red listOrange JuiceSource
Refusal charges, in plain English
- PESTICIDE1 refused line
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 Mas-Pex
- Is Mas-Pex on an FDA import alert?
- Yes. As of October 26, 2026, Mas-Pex is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for orange juice; FDA published the listing on June 7, 2012.
- Has FDA refused shipments from Mas-Pex?
- Yes. FDA refused 1 shipment line from Mas-Pex on July 26, 2024. The most recent, on July 26, 2024, was orange, citrus fruit juices or concentrates, charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Mas-Pex's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 1 line).
- What is Mas-Pex's FEI number?
- Mas-Pex's FDA Establishment Identifier (FEI) is 3014018069.
- Can shipments from Mas-Pex still enter the U.S.?
- Shipments of orange juice from Mas-Pex can be detained without physical examination under Import Alert 99-08; 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.