Lacteos de Agalta
FDA import alert and refusal historySan Esteban, HondurasFEI 3006852601
As of October 26, 2026, Lacteos de Agalta (San Esteban, Honduras) is on the red list of FDA Import Alert 99-43 (Ready-to-eat foods: insanitary conditions) for semi dry cheese, published by FDA on August 6, 2026, and has 5 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-43 · red list
- Last import refusal
- Cheese products, standardized, n.e.c. · LIST INGRE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Lacteos de Agalta
6 records, newest first. Each line links to the FDA page it came from.
2026
- Import refusalRefused, Cheese products, standardized, n.e.c.LIST INGREINSANITARYLACKS FIRMLACKS N/CUSUAL NAMELABELINGNUTRIT LBLEntry 8QB-0001362-6Source
- Import refusalRefused, Cheese products, standardized, n.e.c.INSANITARYEntry 8QB-0001336-0Source
- Import refusalRefused, Cheese products, standardized, n.e.c.LIST INGRELACKS FIRMLACKS N/CUSUAL NAMEALLERGENLABELINGNUTRIT LBLEntry 8QB-0001357-6Source
- Import alert listingListed on Import Alert 99-43red listSemi Dry CheeseSource
- Import refusalRefused, Cheese products, standardized, n.e.c.INSANITARYMFR INSANMFR INJEntry 8QB-0001363-4Source
2022
- Import refusalRefused, Cheese, pasteurized, process (standardized)NO ENGLISHEntry 9AG-0057615-9Source
Refusal charges, in plain English
- INSANITARY3 refused lines
Prepared, packed or held under insanitary conditions
The product appeared to have been prepared, packed, or held under insanitary conditions whereby it may have been contaminated with filth or rendered injurious to health.
- LABELING2 refused lines
Fair Packaging and Labeling Act
The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.
- LACKS FIRM2 refused lines
Manufacturer name and address missing
The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.
- LACKS N/C2 refused lines
Net quantity statement missing
The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.
- LIST INGRE2 refused lines
Ingredients not listed
The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).
- NUTRIT LBL2 refused lines
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
- USUAL NAME2 refused lines
Common or usual name missing
The label appeared not to show the common or usual name of the food.
- ALLERGEN1 refused line
Major food allergen not declared
The label appeared not to declare all major food allergens present in the product, as section 403(w) of the FD&C Act requires.
Questions about Lacteos de Agalta
- Is Lacteos de Agalta on an FDA import alert?
- Yes. As of October 26, 2026, Lacteos de Agalta is on the red list of FDA Import Alert 99-43, “Ready-to-eat foods: insanitary conditions”, for semi dry cheese; FDA published the listing on August 6, 2026.
- Has FDA refused shipments from Lacteos de Agalta?
- Yes. FDA refused 5 shipment lines from Lacteos de Agalta between December 9, 2022 and August 26, 2026. The most recent, on August 26, 2026, was cheese products, standardized, n.e.c., charged as LIST INGRE (ingredients not listed).
- Why did FDA refuse Lacteos de Agalta's shipments?
- The most frequent charges are INSANITARY (prepared, packed or held under insanitary conditions, 3 lines) and LABELING (fair packaging and labeling act, 2 lines).
- What is Lacteos de Agalta's FEI number?
- Lacteos de Agalta's FDA Establishment Identifier (FEI) is 3006852601.
- Can shipments from Lacteos de Agalta still enter the U.S.?
- Shipments of semi dry cheese from Lacteos de Agalta can be detained without physical examination under Import Alert 99-43; 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.