Planta de Procesos GM, S.A. de C.V.
FDA import alert and refusal historyAhome, MexicoFEI 3011289698
As of October 26, 2026, Planta de Procesos GM, S.A. de C.V. (Ahome, Mexico) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for shrimp w/coconut; shrimp w/cheese and bacon; shrimp patties "hamburguesa de camaron, published by FDA on March 19, 2021, and has 10 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
- Aquaculture harvested fishery/seafood products, n.e.c., · SALMONELLA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Planta de Procesos GM, S.A. de C.V.
11 records, newest first. Each line links to the FDA page it came from.
2022
- Import refusalRefused, Aquaculture harvested fishery/seafood products, n.e.c.,SALMONELLAEntry 92Q-0016836-8Source
- Import refusalRefused, Aquaculture harvested fishery/seafood products, n.e.c.,SALMONELLAEntry 92Q-0016719-6Source
- Import refusalRefused, Shrimp and prawns, aquaculture harvested fishery/seafood productsSALMONELLAEntry 92Q-0016836-8Source
- Import refusalRefused, Aquaculture harvested fishery/seafood products, n.e.c.,SALMONELLAEntry 92Q-0016725-3Source
- Import refusalSource
Refused, 2 lines in one entry: Aquaculture harvested fishery/seafood products, n.e.c.,; Shrimp and prawns, aquaculture harvested fishery/seafood productsSALMONELLAEntry 92Q-0016814-5Show 2 linesHide lines
- Refused, Aquaculture harvested fishery/seafood products, n.e.c.,SALMONELLAEntry 92Q-0016814-5Source
- Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsSALMONELLAEntry 92Q-0016814-5Source
- Import refusalSource
Refused, 2 lines in one entry: Shrimp and prawns, aquaculture harvested fishery/seafood productsSALMONELLAEntry 92Q-0017144-6Show 2 linesHide lines
- Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsSALMONELLAEntry 92Q-0017144-6Source
- Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsSALMONELLAEntry 92Q-0017144-6Source
- Import refusalRefused, Shrimp & prawnsSALMONELLAEntry 92Q-0016797-2Source
2021
- Import alert listingListed on Import Alert 16-81red listShrimp w/coconut; Shrimp w/cheese and bacon; Shrimp Patties "Hamburguesa de CamaronSource
- Import refusalRefused, Meals separated in serving container with crustaceans (e.g., crab, crayfish, lobster, shrimp/prawns)SALMONELLAEntry 92Q-0014009-4Source
Refusal charges, in plain English
- SALMONELLA10 refused lines
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 Planta de Procesos GM, S.A. de C.V.
- Is Planta de Procesos GM, S.A. de C.V. on an FDA import alert?
- Yes. As of October 26, 2026, Planta de Procesos GM, S.A. de C.V. is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for shrimp w/coconut; shrimp w/cheese and bacon; shrimp patties "hamburguesa de camaron; FDA published the listing on March 19, 2021.
- Has FDA refused shipments from Planta de Procesos GM, S.A. de C.V.?
- Yes. FDA refused 10 shipment lines from Planta de Procesos GM, S.A. de C.V. between March 10, 2021 and April 28, 2022. The most recent, on April 28, 2022, was aquaculture harvested fishery/seafood products, n.e.c.,, charged as SALMONELLA (salmonella).
- Why did FDA refuse Planta de Procesos GM, S.A. de C.V.'s shipments?
- The most frequent charge is SALMONELLA (salmonella, 10 lines).
- What is Planta de Procesos GM, S.A. de C.V.'s FEI number?
- Planta de Procesos GM, S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3011289698.
- Can shipments from Planta de Procesos GM, S.A. de C.V. still enter the U.S.?
- Shipments of shrimp w/coconut; shrimp w/cheese and bacon; shrimp patties "hamburguesa de camaron from Planta de Procesos GM, 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.