Ghandour & Sons Est.
FDA import alert and refusal historyBeyrouth, LebanonFEI 3012010781
Recorded by FDA as GHANDOUR & SONS EST.
As of October 25, 2026, Ghandour & Sons Est. (Beyrouth, Lebanon) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for halawa plain; tahini/tahina ground sesame seed paste; tahini sauce; halawa sugar free; halawa w/pistachio; halawa w/ pisachio, published by FDA on September 16, 2009, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-19 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Ghandour & Sons Est.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-19red listHalawa plain; Tahini/Tahina ground sesame seed paste; Tahini Sauce; Halawa Sugar Free; Halawa w/pistachio; Halawa w/ PisachioSource
Questions about Ghandour & Sons Est.
- Is Ghandour & Sons Est. on an FDA import alert?
- Yes. As of October 25, 2026, Ghandour & Sons Est. is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for halawa plain; tahini/tahina ground sesame seed paste; tahini sauce; halawa sugar free; halawa w/pistachio; halawa w/ pisachio; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Ghandour & Sons Est.?
- No FDA import refusals for Ghandour & Sons Est. appear in FDA's refusal data since October 2016, as of October 25, 2026.
- What is Ghandour & Sons Est.'s FEI number?
- Ghandour & Sons Est.'s FDA Establishment Identifier (FEI) is 3012010781.
- Can shipments from Ghandour & Sons Est. still enter the U.S.?
- Shipments of halawa plain; tahini/tahina ground sesame seed paste; tahini sauce; halawa sugar free; halawa w/pistachio; halawa w/ pisachio from Ghandour & Sons Est. can be detained without physical examination under Import Alert 99-19; 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.