PLANTAS MEDICINALES
⚠️ High Risk
FEI: 3030489492 • Temecula, CA • UNITED STATES
FEI Number
3030489492
Location
Temecula, CA
Country
UNITED STATESAddress
42015 Remington Ave, Ste 107, Temecula, CA, United States
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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).
NO ENGLISH
Required label or labeling appears to not be in English in violation of 21 C.F.R. 801.15(c)(1)
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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)).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/14/2025 | 54KCY14GLUCOSAMINE HYDROCHLORIDE (HERBAL AND BOTANICALS, NOT TEAS II) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 6/11/2025 | 54YCT99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 5/28/2025 | 54FCA10GARLIC (HERBAL & BOTANICALS, NOT TEAS) | 473LABELING | Division of Southeast Imports (DSEI) |
| 5/28/2025 | 54ACY13VITAMIN C (ASCORBIC ACID) | 473LABELING | Division of Southeast Imports (DSEI) |
| 3/20/2025 | 54HCY05OMEGA-3 (FATS AND LIPID SUBSTANCES) | Division of Southeast Imports (DSEI) | |
| 3/20/2025 | 54HCY05OMEGA-3 (FATS AND LIPID SUBSTANCES) | Division of Southeast Imports (DSEI) | |
| 9/20/2024 | 54ACY13VITAMIN C (ASCORBIC ACID) | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is PLANTAS MEDICINALES's FDA import refusal history?
PLANTAS MEDICINALES (FEI: 3030489492) has 7 FDA import refusal record(s) in our database, spanning from 9/20/2024 to 7/14/2025.
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. PLANTAS MEDICINALES's FEI number is 3030489492.
What types of violations has PLANTAS MEDICINALES received?
PLANTAS MEDICINALES has been cited for 4 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 PLANTAS MEDICINALES come from?
All FDA import refusal data for PLANTAS MEDICINALES 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.