Bumble Bee Mexico, S. de R.L. de C.V.
⚠️ Moderate Risk
FEI: 3024353964 • Puerto Madero, Chiapas • MEXICO
FEI Number
3024353964
Location
Puerto Madero, Chiapas
Country
MEXICOAddress
Av. Central Sur Mza. C Y E, Lte. 3 Y 4, Col. Puerto Madero Centro, Tapachula, Puerto Madero, Chiapas, Mexico
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
FALSE
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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/5/2023 | 16AEF45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | Division of Southwest Imports (DSWI) | |
| 12/5/2023 | 16AEF45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | Division of Southwest Imports (DSWI) | |
| 12/5/2023 | 16AEF45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | Division of Southwest Imports (DSWI) | |
| 12/5/2023 | 16AEF45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | Division of Southwest Imports (DSWI) | |
| 12/4/2023 | 16AEF45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | Division of Southwest Imports (DSWI) | |
| 11/14/2023 | 16AEF45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | Division of Southwest Imports (DSWI) | |
| 11/14/2023 | 16AEF45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | Division of Southwest Imports (DSWI) | |
| 11/14/2023 | 16AEF45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | Division of Southwest Imports (DSWI) | |
| 11/14/2023 | 16AEF45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | Division of Southwest Imports (DSWI) | |
| 11/14/2023 | 16AEF45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | Division of Southwest Imports (DSWI) | |
| 11/14/2023 | 16AEF45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | Division of Southwest Imports (DSWI) | |
| 11/14/2023 | 16AEF45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | Division of Southwest Imports (DSWI) | |
| 11/14/2023 | 16AEF45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | Division of Southwest Imports (DSWI) |
Frequently Asked Questions
What is Bumble Bee Mexico, S. de R.L. de C.V.'s FDA import refusal history?
Bumble Bee Mexico, S. de R.L. de C.V. (FEI: 3024353964) has 13 FDA import refusal record(s) in our database, spanning from 11/14/2023 to 12/5/2023.
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. Bumble Bee Mexico, S. de R.L. de C.V.'s FEI number is 3024353964.
What types of violations has Bumble Bee Mexico, S. de R.L. de C.V. received?
Bumble Bee Mexico, S. de R.L. de C.V. has been cited for 2 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 Bumble Bee Mexico, S. de R.L. de C.V. come from?
All FDA import refusal data for Bumble Bee Mexico, S. de R.L. de C.V. 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.