Organic Aloe
⚠️ Moderate Risk
FEI: 3004934693 • Albertinia, Western Cape • SOUTH AFRICA
FEI Number
3004934693
Location
Albertinia, Western Cape
Country
SOUTH AFRICAAddress
39 Industrial Avenue, , Albertinia, Western Cape, South Africa
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
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).
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.
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).
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.
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.
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.
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.
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.
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.
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/29/2012 | 29YGB99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C. | Division of Southeast Imports (DSEI) | |
| 4/26/2012 | 66VBY99MISCELLANEOUS PATENT MEDICINES, ETC. | 2280DIRSEXMPT | Division of Northeast Imports (DNEI) |
| 4/26/2012 | 66PBY99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C. | 2280DIRSEXMPT | Division of Northeast Imports (DNEI) |
| 4/26/2012 | 66PBY99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C. | 2280DIRSEXMPT | Division of Northeast Imports (DNEI) |
| 4/26/2012 | 66VBY99MISCELLANEOUS PATENT MEDICINES, ETC. | 2280DIRSEXMPT | Division of Northeast Imports (DNEI) |
| 4/26/2012 | 66VBY99MISCELLANEOUS PATENT MEDICINES, ETC. | 2280DIRSEXMPT | Division of Northeast Imports (DNEI) |
| 4/26/2012 | 66VBY99MISCELLANEOUS PATENT MEDICINES, ETC. | 2280DIRSEXMPT | Division of Northeast Imports (DNEI) |
| 4/26/2012 | 66VBY99MISCELLANEOUS PATENT MEDICINES, ETC. | 2280DIRSEXMPT | Division of Northeast Imports (DNEI) |
| 4/26/2012 | 66VBY99MISCELLANEOUS PATENT MEDICINES, ETC. | 2280DIRSEXMPT | Division of Northeast Imports (DNEI) |
| 4/26/2012 | 31MET99BLENDED TEAS, N.E.C. | Division of Northeast Imports (DNEI) | |
| 4/26/2012 | 66VBY99MISCELLANEOUS PATENT MEDICINES, ETC. | 75UNAPPROVED | Division of Northeast Imports (DNEI) |
| 4/26/2012 | 66VBY99MISCELLANEOUS PATENT MEDICINES, ETC. | 75UNAPPROVED | Division of Northeast Imports (DNEI) |
| 4/26/2012 | 66PBY99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C. | 16DIRECTIONS | Division of Northeast Imports (DNEI) |
| 4/26/2012 | 66VBY99MISCELLANEOUS PATENT MEDICINES, ETC. | 16DIRECTIONS | Division of Northeast Imports (DNEI) |
| 2/10/2011 | 63HBA99CATHARTIC N.E.C. | New York District Office (NYK-DO) | |
| 7/22/2003 | 66VCS99MISCELLANEOUS PATENT MEDICINES, ETC. | New York District Office (NYK-DO) | |
| 7/22/2003 | 66VCS99MISCELLANEOUS PATENT MEDICINES, ETC. | New York District Office (NYK-DO) | |
| 3/31/2003 | 54EYY99HERBALS & BOTANICAL TEAS, N.E.C. | New York District Office (NYK-DO) | |
| 3/31/2003 | 66VCS99MISCELLANEOUS PATENT MEDICINES, ETC. | New York District Office (NYK-DO) | |
| 3/31/2003 | 66VCS99MISCELLANEOUS PATENT MEDICINES, ETC. | New York District Office (NYK-DO) | |
| 3/31/2003 | 66VCS99MISCELLANEOUS PATENT MEDICINES, ETC. | New York District Office (NYK-DO) | |
| 3/31/2003 | 66VCS99MISCELLANEOUS PATENT MEDICINES, ETC. | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Organic Aloe's FDA import refusal history?
Organic Aloe (FEI: 3004934693) has 22 FDA import refusal record(s) in our database, spanning from 3/31/2003 to 5/29/2012.
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. Organic Aloe's FEI number is 3004934693.
What types of violations has Organic Aloe received?
Organic Aloe has been cited for 10 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 Organic Aloe come from?
All FDA import refusal data for Organic Aloe 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.