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Grupo HV S. de R.L. de C.V.

⚠️ Moderate Risk

FEI: 3010630889 • El Progreso, Yoro • HONDURAS

FEI

FEI Number

3010630889

📍

Location

El Progreso, Yoro

🇭🇳

Country

HONDURAS
🏢

Address

Cuadra Y Media De Carretera A Sta. Rita, Colonia Las Palmeras, El Progreso, Yoro, Honduras

Moderate Risk

FDA Import Risk Assessment

37.7
LowModerateHighCritical

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

Statistics

11
Total Refusals
15
Unique Violations
7/12/2013
Latest Refusal
11/20/2009
Earliest Refusal

Score Breakdown

Violation Severity
56.7×40%
Refusal Volume
40.0×30%
Recency
0.0×20%
Frequency
30.2×10%
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

833×

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.

4732×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

3242×

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)).

622×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

3282×

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.

92×

SALMONELLA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.

3212×

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.

1182×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

2181×

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.

3201×

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.

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).

3361×

INCONSPICU

Information required by the Act to be on the label or labeling does not appear to be conspicuous enough as to render it likely to be read and understood by the ordinary individual under customary conditions of purchase and use.

4821×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

751×

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).

Refusal History

DateProductViolationsDivision
7/12/2013
66CAL99STOOL SOFTENER N.E.C.
118NOT LISTED
3280FRNMFGREG
New Orleans District Office (NOL-DO)
6/26/2012
66VBK99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
336INCONSPICU
75UNAPPROVED
New Orleans District Office (NOL-DO)
9/15/2011
37JYT08TOMATO SAUCE (WITH OTHER INGREDIENTS)
62NEEDS FCE
83NO PROCESS
New Orleans District Office (NOL-DO)
9/15/2011
37JYT08TOMATO SAUCE (WITH OTHER INGREDIENTS)
62NEEDS FCE
83NO PROCESS
New Orleans District Office (NOL-DO)
6/9/2011
04BGT02NOODLES, EGG
321LACKS N/C
324NO ENGLISH
328USUAL NAME
482NUTRIT LBL
New Orleans District Office (NOL-DO)
6/9/2011
07BGT06POTATO CHIPS,FRIED
11UNSAFE COL
320LACKS FIRM
328USUAL NAME
New Orleans District Office (NOL-DO)
6/8/2010
28FCY99MIXED SPICE AND SEASONINGS, GROUND, CRACKED, WITHOUT SALT, N.E.C.
9SALMONELLA
New Orleans District Office (NOL-DO)
6/8/2010
28FCY99MIXED SPICE AND SEASONINGS, GROUND, CRACKED, WITHOUT SALT, N.E.C.
9SALMONELLA
New Orleans District Office (NOL-DO)
12/7/2009
24AGE99BEANS, CORN, AND PEA, N.E.C. (VEGETABLE)
83NO PROCESS
New Orleans District Office (NOL-DO)
11/20/2009
07BGT99FRIED SNACK FOODS, N.E.C.
324NO ENGLISH
473LABELING
New Orleans District Office (NOL-DO)
11/20/2009
28BCT16CUMIN, GROUND, CRACKED (SPICE)
218LIST INGRE
321LACKS N/C
473LABELING
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Grupo HV S. de R.L. de C.V.'s FDA import refusal history?

Grupo HV S. de R.L. de C.V. (FEI: 3010630889) has 11 FDA import refusal record(s) in our database, spanning from 11/20/2009 to 7/12/2013.

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. Grupo HV S. de R.L. de C.V.'s FEI number is 3010630889.

What types of violations has Grupo HV S. de R.L. de C.V. received?

Grupo HV S. de R.L. de C.V. has been cited for 15 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 Grupo HV S. de R.L. de C.V. come from?

All FDA import refusal data for Grupo HV S. de R.L. de C.V. 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.