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REHMAT GROUP

⚠️ Moderate Risk

FEI: 3010158972 • Pakistan, Punjab • PAKISTAN

FEI

FEI Number

3010158972

📍

Location

Pakistan, Punjab

🇵🇰

Country

PAKISTAN
🏢

Address

RAILWAY ROAD PASRUR, PASRUR, SIALKOT, Pakistan, Punjab, Pakistan

Moderate Risk

FDA Import Risk Assessment

38.0
LowModerateHighCritical

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

Statistics

14
Total Refusals
14
Unique Violations
8/12/2015
Latest Refusal
11/18/2010
Earliest Refusal

Score Breakdown

Violation Severity
54.8×40%
Refusal Volume
43.6×30%
Recency
0.0×20%
Frequency
29.6×10%
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

94×

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.

2183×

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.

1183×

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).

4823×

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.

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.

162×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

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.

4712×

CSTIC LBLG

The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.

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).

2741×

COLOR LBLG

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

2491×

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.

3211×

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.

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)).

4731×

LABELING

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

Refusal History

DateProductViolationsDivision
8/12/2015
28BGN49TURMERIC, GROUND, CRACKED (SPICE)
9SALMONELLA
Division of Northeast Imports (DNEI)
8/12/2015
28BGN49TURMERIC, GROUND, CRACKED (SPICE)
9SALMONELLA
Division of Northeast Imports (DNEI)
10/27/2014
53IC01DENTIFRICES (AEROSOL, LIQUID, TOOTHPASTES, TOOTHPOWDERS), WITHOUT FLUORIDE (ORAL HYGIENE PRODUCTS)
471CSTIC LBLG
Division of Northeast Imports (DNEI)
10/27/2014
53IC01DENTIFRICES (AEROSOL, LIQUID, TOOTHPASTES, TOOTHPOWDERS), WITHOUT FLUORIDE (ORAL HYGIENE PRODUCTS)
471CSTIC LBLG
Division of Northeast Imports (DNEI)
10/27/2014
63RAJ05SODIUM MONOFLUOROPHOSPHATE (DENTAL CARIES PROPHYLACTIC)
118NOT LISTED
16DIRECTIONS
Division of Northeast Imports (DNEI)
10/27/2014
62SDL99ANTI-SEBORRHEIC N.E.C.
16DIRECTIONS
75UNAPPROVED
Division of Northeast Imports (DNEI)
9/12/2014
21SGT14TAMARIND (SUBTROPICAL AND TROPICAL FRUIT)
249FILTHY
Division of Northeast Imports (DNEI)
9/12/2014
28BAH49TURMERIC, GROUND, CRACKED (SPICE)
9SALMONELLA
Division of Northeast Imports (DNEI)
7/28/2014
07YGT99SNACK FOODS NOT ELSEWHERE MENTIONED, N.E.C.
218LIST INGRE
482NUTRIT LBL
New York District Office (NYK-DO)
7/28/2014
28BGT49TURMERIC, GROUND, CRACKED (SPICE)
9SALMONELLA
New York District Office (NYK-DO)
5/22/2014
63HAS99CATHARTIC N.E.C.
118NOT LISTED
Division of Northeast Imports (DNEI)
5/22/2014
63HAS99CATHARTIC N.E.C.
118NOT LISTED
Division of Northeast Imports (DNEI)
11/18/2010
33YGT99CANDY WITHOUT CHOCOLATE N.E.C.
218LIST INGRE
320LACKS FIRM
324NO ENGLISH
328USUAL NAME
473LABELING
482NUTRIT LBL
New York District Office (NYK-DO)
11/18/2010
07BGT99FRIED SNACK FOODS, N.E.C.
218LIST INGRE
274COLOR LBLG
320LACKS FIRM
321LACKS N/C
328USUAL NAME
482NUTRIT LBL
New York District Office (NYK-DO)

Frequently Asked Questions

What is REHMAT GROUP's FDA import refusal history?

REHMAT GROUP (FEI: 3010158972) has 14 FDA import refusal record(s) in our database, spanning from 11/18/2010 to 8/12/2015.

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. REHMAT GROUP's FEI number is 3010158972.

What types of violations has REHMAT GROUP received?

REHMAT GROUP has been cited for 14 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 REHMAT GROUP come from?

All FDA import refusal data for REHMAT GROUP 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.