GRUPO CALIBEB SA DE CV.
⚠️ High Risk
FEI: 3014726894 • Chihuahua, Chihuahua • MEXICO
FEI Number
3014726894
Location
Chihuahua, Chihuahua
Country
MEXICOAddress
Avenida Nicolas Gogol N. 11342 Int. 37-38, Col. Complejo Industrial Chihuahua, Chihuahua, Chihuahua, Chihuahua, Mexico
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
UNSAFE ADD
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.
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)).
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.
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/28/2024 | 30KGY02BEVERAGE BASE, IMITATION CITRUS, LIQUID | Division of Southwest Imports (DSWI) | |
| 10/28/2024 | 30KGY03BEVERAGE BASE, IMITATION CORE FRUIT, LIQUID | Division of Southwest Imports (DSWI) | |
| 10/28/2024 | 30KGY04BEVERAGE BASE, IMITATION MIXED FRUIT, LIQUID | Division of Southwest Imports (DSWI) | |
| 10/28/2024 | 30KGY02BEVERAGE BASE, IMITATION CITRUS, LIQUID | Division of Southwest Imports (DSWI) | |
| 10/28/2024 | 30KGY02BEVERAGE BASE, IMITATION CITRUS, LIQUID | Division of Southwest Imports (DSWI) | |
| 10/28/2024 | 30KGY01BEVERAGE BASE, IMITATION BERRY, LIQUID | Division of Southwest Imports (DSWI) | |
| 10/28/2024 | 30KGY99IMITATION FRUIT FLAVORED BEVERAGE BASE, LIQUID, N.E.C. | Division of Southwest Imports (DSWI) | |
| 10/28/2024 | 30KGY02BEVERAGE BASE, IMITATION CITRUS, LIQUID | Division of Southwest Imports (DSWI) |
Frequently Asked Questions
What is GRUPO CALIBEB SA DE CV.'s FDA import refusal history?
GRUPO CALIBEB SA DE CV. (FEI: 3014726894) has 8 FDA import refusal record(s) in our database, spanning from 10/28/2024 to 10/28/2024.
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. GRUPO CALIBEB SA DE CV.'s FEI number is 3014726894.
What types of violations has GRUPO CALIBEB SA DE CV. received?
GRUPO CALIBEB SA DE CV. 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 GRUPO CALIBEB SA DE CV. come from?
All FDA import refusal data for GRUPO CALIBEB SA DE CV. 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.