Reliquias del Golfo
⚠️ Moderate Risk
FEI: 3008078281 • El Salvedor, San Salvador • EL SALVADOR
FEI Number
3008078281
Location
El Salvedor, San Salvador
Country
EL SALVADORAddress
15 Av Norte #1317 Colonia Layco, , El Salvedor, San Salvador, El Salvador
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
How is this score calculated?
Proprietary Algorithm
- 40% Violation Severity — AI-assessed (1-10)
- 30% Refusal Volume — Logarithmic scale
- 20% Recency — Decays over 5 years
- 10% Frequency — Refusals per year
© ImportRefusal.com Original Analysis
Violation Summary
LIST INGRE
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
USUAL NAME
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.
LACKS N/C
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
LACKS FIRM
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.
NO PROCESS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
NO ENGLISH
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).
YELLOW #5
The food appears to bear or contain the color additive FD & C Yellow No. 5, which is not declared on the label per 21 CFR 74.705(a)(c) under section 721.
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/22/2019 | 16JGH05SHRIMP & PRAWNS | Division of West Coast Imports (DWCI) | |
| 8/13/2019 | 30YYY04HORCHATA (BEVERAGE BASE N.E.C.) | Division of West Coast Imports (DWCI) | |
| 8/13/2019 | 34FYY01CHOCOLATE CANDY BAR, WITHOUT NUTS AND FRUIT | Division of West Coast Imports (DWCI) | |
| 8/13/2019 | 33LYD05CANDY BAR OR PIECES (NOT CARAMEL OR FONDANT), SOFT, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE) | Division of West Coast Imports (DWCI) | |
| 8/13/2019 | 21TYH48COCONUT, SUBTROPICAL AND TROPICAL FRUIT, DRIED OR PASTE | Division of West Coast Imports (DWCI) | |
| 8/13/2019 | 33LYD05CANDY BAR OR PIECES (NOT CARAMEL OR FONDANT), SOFT, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE) | Division of West Coast Imports (DWCI) | |
| 8/1/2019 | 25YYC99VEGETABLE & VEGETABLE PRODUCTS NOT MENTIONED ELSEWHERE, N.E.C. | 321LACKS N/C | Division of West Coast Imports (DWCI) |
| 8/1/2019 | 20GYC04LEMON (CITRUS) | 249FILTHY | Division of West Coast Imports (DWCI) |
| 8/1/2019 | 33LYD05CANDY BAR OR PIECES (NOT CARAMEL OR FONDANT), SOFT, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE) | Division of West Coast Imports (DWCI) | |
| 8/1/2019 | 20AYD05CURRANTS, BLACK (BERRY) | Division of West Coast Imports (DWCI) | |
| 8/1/2019 | 21TYH48COCONUT, SUBTROPICAL AND TROPICAL FRUIT, DRIED OR PASTE | Division of West Coast Imports (DWCI) | |
| 8/1/2019 | 24AYY99BEANS, CORN, AND PEA, N.E.C. (VEGETABLE) | Division of West Coast Imports (DWCI) | |
| 8/1/2019 | 30YYY04HORCHATA (BEVERAGE BASE N.E.C.) | Division of West Coast Imports (DWCI) | |
| 5/23/2019 | 21XYH14TAMARIND (SUBTROPICAL/TROPICAL FRUIT PULP) | 249FILTHY | Division of West Coast Imports (DWCI) |
| 2/26/2013 | 16AGH30PORGY | 249FILTHY | Atlanta District Office (ATL-DO) |
| 2/26/2013 | 16AGH73MACKEREL (ALL EXCEPT SCOMBEROMORUS SP, EG SPANISH OR KING SEE '22') | 249FILTHY | Atlanta District Office (ATL-DO) |
| 4/6/2011 | 16AFH67CATFISH, SALT WATER | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 4/6/2011 | 16AFH67CATFISH, SALT WATER | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 4/6/2011 | 16AFH67CATFISH, SALT WATER | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 4/6/2011 | 16AFH67CATFISH, SALT WATER | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 12/6/2010 | 16AFH67CATFISH, SALT WATER | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 12/6/2010 | 16RFH03SHRIMP, IMITATION | 83NO PROCESS | Los Angeles District Office (LOS-DO) |
| 10/29/2010 | 24AYY99BEANS, CORN, AND PEA, N.E.C. (VEGETABLE) | 324NO ENGLISH | Los Angeles District Office (LOS-DO) |
| 10/26/2010 | 64HBL99EXPECTORANT N.E.C. | 75UNAPPROVED | Los Angeles District Office (LOS-DO) |
| 10/26/2010 | 64HBL99EXPECTORANT N.E.C. | 75UNAPPROVED | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Reliquias del Golfo's FDA import refusal history?
Reliquias del Golfo (FEI: 3008078281) has 25 FDA import refusal record(s) in our database, spanning from 10/26/2010 to 11/22/2019.
What is an FEI number?
FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Reliquias del Golfo's FEI number is 3008078281.
What types of violations has Reliquias del Golfo received?
Reliquias del Golfo has been cited for 11 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.
Where does this information about Reliquias del Golfo come from?
All FDA import refusal data for Reliquias del Golfo is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.
Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.