Pearl Corporation
FDA import alert and refusal historyHochiminh City, VietnamFEI 3013861049
Recorded by FDA as PEARL CORPORATION
As of October 26, 2026, Pearl Corporation (Hochiminh City, Vietnam) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for lemograss powder, published by FDA on March 13, 2026, 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 99-19 · red list
- Last import refusal
- Lemon grass, ground, cracked (spice) · SALMONELLA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Pearl Corporation
2 records, newest first. Each line links to the FDA page it came from.
2026
- Import refusalRefused, Lemon grass, ground, cracked (spice)SALMONELLAEntry KM6-1643867-7Source
- Import alert listingListed on Import Alert 99-19red listLemograss PowderSource
Refusal charges, in plain English
- SALMONELLA1 refused line
Salmonella
The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
Questions about Pearl Corporation
- Is Pearl Corporation on an FDA import alert?
- Yes. As of October 26, 2026, Pearl Corporation is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for lemograss powder; FDA published the listing on March 13, 2026.
- Has FDA refused shipments from Pearl Corporation?
- Yes. FDA refused 1 shipment line from Pearl Corporation on April 15, 2026. The most recent, on April 15, 2026, was lemon grass, ground, cracked (spice), charged as SALMONELLA (salmonella).
- Why did FDA refuse Pearl Corporation's shipments?
- The most frequent charge is SALMONELLA (salmonella, 1 line).
- What is Pearl Corporation's FEI number?
- Pearl Corporation's FDA Establishment Identifier (FEI) is 3013861049.
- Can shipments from Pearl Corporation still enter the U.S.?
- Shipments of lemograss powder from Pearl Corporation 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.