Ronnie Ben Ephraim
FDA import alert and refusal historyGush Etzion, IsraelFEI 3008160031
As of October 26, 2026, Ronnie Ben Ephraim (Gush Etzion, Israel) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for parsley, published by FDA on February 4, 2013, 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 99-05 · red list
- Last import refusal
- Parsley (leaf & stem vegetable) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Ronnie Ben Ephraim
2 records, newest first. Each line links to the FDA page it came from.
2019
2013
- Import alert listingListed on Import Alert 99-05red listParsleySource
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 Ronnie Ben Ephraim
- Is Ronnie Ben Ephraim on an FDA import alert?
- Yes. As of October 26, 2026, Ronnie Ben Ephraim is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for parsley; FDA published the listing on February 4, 2013.
- Has FDA refused shipments from Ronnie Ben Ephraim?
- Yes. FDA refused 1 shipment line from Ronnie Ben Ephraim on September 30, 2019. The most recent, on September 30, 2019, was parsley (leaf & stem vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Ronnie Ben Ephraim's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 1 line).
- What is Ronnie Ben Ephraim's FEI number?
- Ronnie Ben Ephraim's FDA Establishment Identifier (FEI) is 3008160031.
- Can shipments from Ronnie Ben Ephraim still enter the U.S.?
- Shipments of parsley from Ronnie Ben Ephraim 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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