Omar Plummer
FDA import alert and refusal historyHanover, JamaicaFEI 3015009279
Recorded by FDA as OMAR PLUMMER
As of October 25, 2026, Omar Plummer (Hanover, Jamaica) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for yams fresh; yams, published by FDA on January 4, 2012, 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
- Yams (root & tuber vegetable) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Omar Plummer
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 Omar Plummer
- Is Omar Plummer on an FDA import alert?
- Yes. As of October 25, 2026, Omar Plummer is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for yams fresh; yams; FDA published the listing on January 4, 2012.
- Has FDA refused shipments from Omar Plummer?
- Yes. FDA refused 2 shipment lines from Omar Plummer between November 21, 2022 and October 6, 2023. The most recent, on October 6, 2023, was yams (root & tuber vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Omar Plummer's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Omar Plummer's FEI number?
- Omar Plummer's FDA Establishment Identifier (FEI) is 3015009279.
- Can shipments from Omar Plummer still enter the U.S.?
- Shipments of yams fresh; yams from Omar Plummer 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.