E-Silk Route Ventures (Pvt) Ltd.
FDA import alert and refusal historyRajagiriya, Sri LankaFEI 3013242171
Recorded by FDA as E-SILK ROUTE VENTURES (PVT) LTD.
As of October 25, 2026, E-Silk Route Ventures (Pvt) Ltd. (Rajagiriya, Sri Lanka) is on the red list of FDA Import Alert 99-42 (Foods: heavy metal (toxic element) contamination) for ground cinnamon, published by FDA on February 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 99-42 · red list
- Last import refusal
- Cinnamon, cassia, ground, cracked (spice) · PB-FOOD
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for E-Silk Route Ventures (Pvt) Ltd.
2 records, newest first. Each line links to the FDA page it came from.
2026
- Import alert listingListed on Import Alert 99-42red listGround CinnamonSource
2025
Refusal charges, in plain English
- PB-FOOD1 refused line
PB-FOOD
Questions about E-Silk Route Ventures (Pvt) Ltd.
- Is E-Silk Route Ventures (Pvt) Ltd. on an FDA import alert?
- Yes. As of October 25, 2026, E-Silk Route Ventures (Pvt) Ltd. is on the red list of FDA Import Alert 99-42, “Foods: heavy metal (toxic element) contamination”, for ground cinnamon; FDA published the listing on February 13, 2026.
- Has FDA refused shipments from E-Silk Route Ventures (Pvt) Ltd.?
- Yes. FDA refused 1 shipment line from E-Silk Route Ventures (Pvt) Ltd. on November 18, 2025. The most recent, on November 18, 2025, was cinnamon, cassia, ground, cracked (spice), charged as PB-FOOD (pb-food).
- Why did FDA refuse E-Silk Route Ventures (Pvt) Ltd.'s shipments?
- The most frequent charge is PB-FOOD (pb-food, 1 line).
- What is E-Silk Route Ventures (Pvt) Ltd.'s FEI number?
- E-Silk Route Ventures (Pvt) Ltd.'s FDA Establishment Identifier (FEI) is 3013242171.
- Can shipments from E-Silk Route Ventures (Pvt) Ltd. still enter the U.S.?
- Shipments of ground cinnamon from E-Silk Route Ventures (Pvt) Ltd. can be detained without physical examination under Import Alert 99-42; 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.