Mapeks Gida Ve Sanayi
FDA import alert and refusal historyIzmir, TurkeyFEI 3012311957
As of October 26, 2026, Mapeks Gida Ve Sanayi (IZMIR, Turkey) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for strawberry puree, published by FDA on October 12, 2023, and has 4 FDA import refusals 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
- Strawberries (berry) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Mapeks Gida Ve Sanayi
5 records, newest first. Each line links to the FDA page it came from.
2023
2021
Refusal charges, in plain English
- PESTICIDE4 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 Mapeks Gida Ve Sanayi
- Is Mapeks Gida Ve Sanayi on an FDA import alert?
- Yes. As of October 26, 2026, Mapeks Gida Ve Sanayi is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for strawberry puree; FDA published the listing on October 12, 2023.
- Has FDA refused shipments from Mapeks Gida Ve Sanayi?
- Yes. FDA refused 4 shipment lines from Mapeks Gida Ve Sanayi between May 13, 2021 and August 9, 2023. The most recent, on August 9, 2023, was strawberries (berry), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Mapeks Gida Ve Sanayi's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 4 lines).
- What is Mapeks Gida Ve Sanayi's FEI number?
- Mapeks Gida Ve Sanayi's FDA Establishment Identifier (FEI) is 3012311957.
- Can shipments from Mapeks Gida Ve Sanayi still enter the U.S.?
- Shipments of strawberry puree from Mapeks Gida Ve Sanayi 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.