ImportRefusal LogoImportRefusal

Reliquias del Golfo

⚠️ Moderate Risk

FEI: 3008078281 • El Salvedor, San Salvador • EL SALVADOR

FEI

FEI Number

3008078281

📍

Location

El Salvedor, San Salvador

🇸🇻
🏢

Address

15 Av Norte #1317 Colonia Layco, , El Salvedor, San Salvador, El Salvador

Moderate Risk

FDA Import Risk Assessment

40.8
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

25
Total Refusals
11
Unique Violations
11/22/2019
Latest Refusal
10/26/2010
Earliest Refusal

Score Breakdown

Violation Severity
55.7×40%
Refusal Volume
52.4×30%
Recency
0.0×20%
Frequency
27.5×10%
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

21811×

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.

2499×

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.

3287×

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.

3216×

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.

752×

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).

3202×

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.

831×

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.

2741×

COLOR LBLG

The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.

3241×

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)).

641×

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.

111×

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

DateProductViolationsDivision
11/22/2019
16JGH05SHRIMP & PRAWNS
11UNSAFE COL
218LIST INGRE
274COLOR LBLG
328USUAL NAME
64YELLOW #5
Division of West Coast Imports (DWCI)
8/13/2019
30YYY04HORCHATA (BEVERAGE BASE N.E.C.)
218LIST INGRE
321LACKS N/C
328USUAL NAME
Division of West Coast Imports (DWCI)
8/13/2019
34FYY01CHOCOLATE CANDY BAR, WITHOUT NUTS AND FRUIT
218LIST INGRE
321LACKS N/C
Division of West Coast Imports (DWCI)
8/13/2019
33LYD05CANDY BAR OR PIECES (NOT CARAMEL OR FONDANT), SOFT, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
218LIST INGRE
321LACKS N/C
Division of West Coast Imports (DWCI)
8/13/2019
21TYH48COCONUT, SUBTROPICAL AND TROPICAL FRUIT, DRIED OR PASTE
218LIST INGRE
321LACKS N/C
Division of West Coast Imports (DWCI)
8/13/2019
33LYD05CANDY BAR OR PIECES (NOT CARAMEL OR FONDANT), SOFT, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
218LIST INGRE
321LACKS N/C
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)
218LIST INGRE
328USUAL NAME
Division of West Coast Imports (DWCI)
8/1/2019
20AYD05CURRANTS, BLACK (BERRY)
218LIST INGRE
328USUAL NAME
Division of West Coast Imports (DWCI)
8/1/2019
21TYH48COCONUT, SUBTROPICAL AND TROPICAL FRUIT, DRIED OR PASTE
218LIST INGRE
328USUAL NAME
Division of West Coast Imports (DWCI)
8/1/2019
24AYY99BEANS, CORN, AND PEA, N.E.C. (VEGETABLE)
218LIST INGRE
320LACKS FIRM
328USUAL NAME
Division of West Coast Imports (DWCI)
8/1/2019
30YYY04HORCHATA (BEVERAGE BASE N.E.C.)
218LIST INGRE
320LACKS FIRM
328USUAL NAME
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.