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DO NOT AGE

⚠️ High Risk

FEI: 3018828305 • Derby • UNITED KINGDOM

FEI

FEI Number

3018828305

📍

Location

Derby

🇬🇧
🏢

Address

Unit 4, Melbourne Busine, Derby, , United Kingdom

High Risk

FDA Import Risk Assessment

63.1
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

24
Total Refusals
9
Unique Violations
10/8/2024
Latest Refusal
7/2/2021
Earliest Refusal

Score Breakdown

Violation Severity
63.3×40%
Refusal Volume
51.8×30%
Recency
74.5×20%
Frequency
73.4×10%
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

7519×

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).

4826×

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.

38644×

NCONTACT

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(y) of the FD&C Act in that the dietary supplement label fails to bear a domestic address or phone number through which the responsible person (as described in section 761 of the FD&C Act) may receive a report of a serious adverse event with such dietary supplement.

23004×

DIETARYLBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(B) of the FD&C Act in that the label or labeling fails to identify the product by using the term "dietary supplement", which term may be modified with the name of such an ingredient.

2564×

INCONSPICU

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)).

38622×

DIETARYING

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(A) of the FD&C Act in that the dietary supplement label or labeling fails to list the name of each dietary ingredient of the supplement and the quantity of each such dietary ingredient or , with respect to a proprietary blend of such dietary ingredients, the total quantity of all dietary ingredients in the blend.

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).

38631×

PLANT PART

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(C) of the FD&C Act in that the supplement contains an herb or other botanical described in section 201(ff)(1)(C), and the label or labeling of the supplement fails to identify any part of the plant from which the ingredient is derived.

22801×

DIRSEXMPT

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a drug within the meaning of Section 201(g) and it lacks adequate directions for use.

Refusal History

DateProductViolationsDivision
10/8/2024
66VAY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
10/8/2024
66VAY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
10/8/2024
66VAY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
10/8/2024
66VAY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
10/8/2024
66VAY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
10/8/2024
66VAY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
8/22/2024
54ABY03VITAMIN B2 (RIBOFLAVIN)
3864NCONTACT
482NUTRIT LBL
75UNAPPROVED
Division of Southeast Imports (DSEI)
8/22/2024
54ABY03VITAMIN B2 (RIBOFLAVIN)
3864NCONTACT
482NUTRIT LBL
75UNAPPROVED
Division of Southeast Imports (DSEI)
8/22/2024
54ABY03VITAMIN B2 (RIBOFLAVIN)
3864NCONTACT
482NUTRIT LBL
75UNAPPROVED
Division of Southeast Imports (DSEI)
8/22/2024
54YBA99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
3864NCONTACT
482NUTRIT LBL
75UNAPPROVED
Division of Southeast Imports (DSEI)
8/22/2024
41YGT99DIETARY CONVENTIONAL FOODS, N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
8/9/2024
54AIY07NICOTINAMIDE (NIACINAMIDE) (VITAMIN)
75UNAPPROVED
Division of Southeast Imports (DSEI)
8/9/2024
54AIY07NICOTINAMIDE (NIACINAMIDE) (VITAMIN)
75UNAPPROVED
Division of Southeast Imports (DSEI)
8/5/2024
54AIR07NICOTINAMIDE (NIACINAMIDE) (VITAMIN)
75UNAPPROVED
Division of Southeast Imports (DSEI)
8/5/2024
54YBY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
8/5/2024
54ABR06NIACIN (NICOTINIC ACID) (VITAMIN)
75UNAPPROVED
Division of Southeast Imports (DSEI)
1/13/2023
54YCY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
2300DIETARYLBL
256INCONSPICU
3863PLANT PART
75UNAPPROVED
Division of Southeast Imports (DSEI)
1/13/2023
54YCY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
2300DIETARYLBL
256INCONSPICU
Division of Southeast Imports (DSEI)
1/13/2023
54ADF07NICOTINAMIDE (NIACINAMIDE) (VITAMIN)
2300DIETARYLBL
256INCONSPICU
Division of Southeast Imports (DSEI)
1/13/2023
54YCY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
2300DIETARYLBL
256INCONSPICU
Division of Southeast Imports (DSEI)
1/13/2023
65CCF04BETAINE ANHYDROUS (NUTRIENT/TONIC)
118NOT LISTED
2280DIRSEXMPT
75UNAPPROVED
Division of Southeast Imports (DSEI)
1/13/2023
66VIF99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/2/2021
54ACH07NICOTINAMIDE (NIACINAMIDE) (VITAMIN)
3862DIETARYING
482NUTRIT LBL
Division of Southeast Imports (DSEI)
7/2/2021
54YCH99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
3862DIETARYING
482NUTRIT LBL
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is DO NOT AGE's FDA import refusal history?

DO NOT AGE (FEI: 3018828305) has 24 FDA import refusal record(s) in our database, spanning from 7/2/2021 to 10/8/2024.

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. DO NOT AGE's FEI number is 3018828305.

What types of violations has DO NOT AGE received?

DO NOT AGE has been cited for 9 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 DO NOT AGE come from?

All FDA import refusal data for DO NOT AGE 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.