SILE S.A de C.V
FDA import alert and refusal historyEl Progreso, HondurasFEI 3017516112
As of October 26, 2026, SILE S.A de C.V is not on any FDA import alert in SupplierRadar's records; FDA refused 12 of its shipment lines between November 21, 2022 and June 16, 2025, most often for filthy, putrid or decomposed substance (FILTHY).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Gel cups, fruit flavored · CHOKE HZRD
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for SILE S.A de C.V
12 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalRefused, Gel cups, fruit flavoredCHOKE HZRDEntry DM4-0637669-7Source
2024
- Import refusalSource
Refused, 2 lines in one entry: Corn chips, friedNO ENGLISHEntry E84-0113542-9Show 2 linesHide lines
- Refused, Corn chips, friedNO ENGLISHEntry E84-0113542-9Source
- Refused, Corn chips, friedNO ENGLISHEntry E84-0113542-9Source
2023
- Import refusalSource
Refused, 2 lines in one entry: Gel cups, fruit flavoredFILTHYEntry DM4-0634062-8Show 2 linesHide lines
- Import refusalSource
Refused, 2 lines in one entry: Condiments, n.e.c.; Brown sauceLACKS N/CNO ENGLISHNUTRIT LBLEntry DM4-0635708-5Show 2 linesHide lines
- Refused, Condiments, n.e.c.LACKS N/CNO ENGLISHNUTRIT LBLEntry DM4-0635708-5Source
- Refused, Brown sauceLACKS N/CNO ENGLISHNUTRIT LBLEntry DM4-0635708-5Source
- Import refusalRefused, Gel cups, fruit flavoredFILTHYEntry DM4-0635708-5Source
- Import refusalRefused, Gel cups, fruit flavoredFILTHYNUTRIT LBLEntry DM4-0630108-3Source
- Import refusalRefused, Tomatoes, juiceNO ENGLISHEntry DM4-0629856-0Source
2022
- Import refusalRefused, Gel cups, fruit flavoredSTD QUALITCOLOR LBLGLABELINGEntry DM4-0614987-0Source
- Import refusalRefused, Gel cups, fruit flavoredUNSAFE COLFILTHYLACKS N/CEntry DM4-0616817-7Source
Refusal charges, in plain English
- FILTHY5 refused lines
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.
- NO ENGLISH5 refused lines
Required label information not in English
Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.
- LACKS N/C3 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.
- NUTRIT LBL3 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.
- CHOKE HZRD1 refused line
CHOKE HZRD
- COLOR LBLG1 refused line
Artificial coloring not declared
The product appeared to contain an artificial coloring without labeling that states that fact.
- LABELING1 refused line
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.
- STD QUALIT1 refused line
STD QUALIT
Questions about SILE S.A de C.V
- Is SILE S.A de C.V on an FDA import alert?
- No listing for SILE S.A de C.V appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Honduras page.
- Has FDA refused shipments from SILE S.A de C.V?
- Yes. FDA refused 12 shipment lines from SILE S.A de C.V between November 21, 2022 and June 16, 2025. The most recent, on June 16, 2025, was gel cups, fruit flavored, charged as CHOKE HZRD (choke hzrd).
- Why did FDA refuse SILE S.A de C.V's shipments?
- The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 5 lines) and NO ENGLISH (required label information not in english, 5 lines).
- What is SILE S.A de C.V's FEI number?
- SILE S.A de C.V's FDA Establishment Identifier (FEI) is 3017516112.
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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.