Baja Scallops S DE RL DE CV
FDA import alert and refusal historyCiudad Constitucion, MexicoFEI 3009866413
As of October 26, 2026, Baja Scallops S DE RL DE CV (Ciudad Constitucion, Mexico) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for scallop, published by FDA on February 14, 2022, 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 16-81 · red list
- Last import refusal
- Scallops · SALMONELLA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Baja Scallops S DE RL DE CV
2 records, newest first. Each line links to the FDA page it came from.
2022
- Import refusalRefused, ScallopsSALMONELLAEntry BRQ-0307703-0Source
- Import alert listingListed on Import Alert 16-81red listScallopSource
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 Baja Scallops S DE RL DE CV
- Is Baja Scallops S DE RL DE CV on an FDA import alert?
- Yes. As of October 26, 2026, Baja Scallops S DE RL DE CV is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for scallop; FDA published the listing on February 14, 2022.
- Has FDA refused shipments from Baja Scallops S DE RL DE CV?
- Yes. FDA refused 1 shipment line from Baja Scallops S DE RL DE CV on February 24, 2022. The most recent, on February 24, 2022, was scallops, charged as SALMONELLA (salmonella).
- Why did FDA refuse Baja Scallops S DE RL DE CV's shipments?
- The most frequent charge is SALMONELLA (salmonella, 1 line).
- What is Baja Scallops S DE RL DE CV's FEI number?
- Baja Scallops S DE RL DE CV's FDA Establishment Identifier (FEI) is 3009866413.
- Can shipments from Baja Scallops S DE RL DE CV still enter the U.S.?
- Shipments of scallop from Baja Scallops S DE RL DE CV 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.