Comercializadora Puerto Morelos S.A De C.V.
FDA import alert and refusal historyPuerto Morelos Quintana Roo, MexicoFEI 3002740057
As of October 26, 2026, Comercializadora Puerto Morelos S.A De C.V. (Puerto Morelos Quintana Roo, Mexico) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for lobster; spiny lobster, rock lobster; slipper lobster, published by FDA on September 18, 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 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 Comercializadora Puerto Morelos S.A De C.V.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 16-81red listLobster; Spiny Lobster, Rock Lobster; Slipper LobsterSource
Questions about Comercializadora Puerto Morelos S.A De C.V.
- Is Comercializadora Puerto Morelos S.A De C.V. on an FDA import alert?
- Yes. As of October 26, 2026, Comercializadora Puerto Morelos S.A De C.V. is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for lobster; spiny lobster, rock lobster; slipper lobster; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Comercializadora Puerto Morelos S.A De C.V.?
- No FDA import refusals for Comercializadora Puerto Morelos S.A De C.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Comercializadora Puerto Morelos S.A De C.V.'s FEI number?
- Comercializadora Puerto Morelos S.A De C.V.'s FDA Establishment Identifier (FEI) is 3002740057.
- Can shipments from Comercializadora Puerto Morelos S.A De C.V. still enter the U.S.?
- Shipments of lobster; spiny lobster, rock lobster; slipper lobster from Comercializadora Puerto Morelos S.A De C.V. can be detained without physical examination under Import Alert 16-81; 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.