Productos del Lago Barranquitas, C.A.
FDA import alert and refusal historyLa Canada De Urdaneta, VenezuelaFEI 3010138016
Recorded by FDA as PRODUCTOS DEL LAGO BARRANQUITAS, C.A.
As of October 26, 2026, Productos del Lago Barranquitas, C.A. (La Canada De Urdaneta, Venezuela) is on the red list of FDA Import Alert 16-39 (Ready-to-eat seafood: Listeria monocytogenes) for crab meat, published by FDA on September 6, 2018, is also listed on Import Alert 16-81 (red list), 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 16-39 · red listIA 16-81 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Productos del Lago Barranquitas, C.A.
2 records, newest first. Each line links to the FDA page it came from.
2018
- Import alert listingListed on Import Alert 16-39red listCrab MeatSource
2016
- Import alert listingListed on Import Alert 16-81red listCrabSource
Questions about Productos del Lago Barranquitas, C.A.
- Is Productos del Lago Barranquitas, C.A. on an FDA import alert?
- Yes. As of October 26, 2026, Productos del Lago Barranquitas, C.A. is on the red list of FDA Import Alert 16-39, “Ready-to-eat seafood: Listeria monocytogenes”, for crab meat; FDA published the listing on September 6, 2018.
- Has FDA refused shipments from Productos del Lago Barranquitas, C.A.?
- No FDA import refusals for Productos del Lago Barranquitas, C.A. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Productos del Lago Barranquitas, C.A.'s FEI number?
- Productos del Lago Barranquitas, C.A.'s FDA Establishment Identifier (FEI) is 3010138016.
- Can shipments from Productos del Lago Barranquitas, C.A. still enter the U.S.?
- Shipments of crab meat from Productos del Lago Barranquitas, C.A. can be detained without physical examination under Import Alert 16-39; 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.