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Lankan Delight

FDA import alert and refusal historyGampaha District, Sri LankaFEI 3004856210

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Example subjectLankan Deligh added to Import Alert 16-129 (red list)

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As of October 26, 2026, Lankan Delight (Gampaha District, Sri Lanka) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for curry powder, without salt; curry powder, ground, cracked, without salt, 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

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for Lankan Delight

1 record, newest first. Each line links to the FDA page it came from.

2009

  1. Import alert listing
    Listed on Import Alert 99-19red listCurry Powder, without Salt; Curry Powder, Ground, Cracked, without Salt
    Source

Questions about Lankan Delight

Is Lankan Delight on an FDA import alert?
Yes. As of October 26, 2026, Lankan Delight is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for curry powder, without salt; curry powder, ground, cracked, without salt; FDA published the listing on September 16, 2009.
Has FDA refused shipments from Lankan Delight?
No FDA import refusals for Lankan Delight appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Lankan Delight's FEI number?
Lankan Delight's FDA Establishment Identifier (FEI) is 3004856210.
Can shipments from Lankan Delight still enter the U.S.?
Shipments of curry powder, without salt; curry powder, ground, cracked, without salt from Lankan Delight 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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Example subjectLankan Deligh added to Import Alert 16-129 (red list)

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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.