BETAPAC MANUFACTURER COMPANY LIMITED
⚠️ High Risk
FEI: 3014100495 • St. Catherine, JM-14 • JAMAICA
FEI Number
3014100495
Location
St. Catherine, JM-14
Country
JAMAICAAddress
Lot 20, Twickenham Park Industrial Estate, Spanish Town, St. Catherine, JM-14, Jamaica
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
SALMONELLA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.
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)).
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.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/3/2025 | 28FGT04CURRY POWDER, GROUND, CRACKED, WITHOUT SALT | 9SALMONELLA | Division of Northeast Imports (DNEI) |
| 10/20/2025 | 28FGT04CURRY POWDER, GROUND, CRACKED, WITHOUT SALT | 9SALMONELLA | Division of Southeast Imports (DSEI) |
| 7/23/2025 | 27YCE06PEPPER SAUCE (HOT, MILD, ETC.) | 482NUTRIT LBL | Division of Southeast Imports (DSEI) |
| 7/23/2025 | 27YCE06PEPPER SAUCE (HOT, MILD, ETC.) | Division of Southeast Imports (DSEI) | |
| 8/27/2024 | 28EHT04CURRY POWDER, WITHOUT SALT | 9SALMONELLA | Division of Southeast Imports (DSEI) |
| 1/25/2024 | 28EGT04CURRY POWDER, WITHOUT SALT | 9SALMONELLA | Division of Southeast Imports (DSEI) |
| 6/9/2022 | 28EGT04CURRY POWDER, WITHOUT SALT | 9SALMONELLA | Division of Southeast Imports (DSEI) |
| 1/18/2022 | 28EGT04CURRY POWDER, WITHOUT SALT | 9SALMONELLA | Division of Southeast Imports (DSEI) |
| 4/6/2021 | 28EHT04CURRY POWDER, WITHOUT SALT | 9SALMONELLA | Division of Southeast Imports (DSEI) |
| 4/6/2021 | 28EHT04CURRY POWDER, WITHOUT SALT | 9SALMONELLA | Division of Southeast Imports (DSEI) |
| 7/23/2020 | 28EHT04CURRY POWDER, WITHOUT SALT | 9SALMONELLA | Division of Southeast Imports (DSEI) |
| 10/23/2018 | 28EHT04CURRY POWDER, WITHOUT SALT | 9SALMONELLA | Division of Southeast Imports (DSEI) |
| 10/23/2018 | 28EHT04CURRY POWDER, WITHOUT SALT | 9SALMONELLA | Division of Southeast Imports (DSEI) |
| 7/6/2015 | 28EGE04CURRY POWDER, WITHOUT SALT | 9SALMONELLA | Florida District Office (FLA-DO) |
| 8/22/2013 | 28EGT04CURRY POWDER, WITHOUT SALT | 9SALMONELLA | Division of Northeast Imports (DNEI) |
| 8/22/2013 | 28EGT04CURRY POWDER, WITHOUT SALT | 9SALMONELLA | Division of Northeast Imports (DNEI) |
| 7/29/2013 | 27YHY99CONDIMENTS, N.E.C. | 9SALMONELLA | Florida District Office (FLA-DO) |
| 7/29/2013 | 27YHY99CONDIMENTS, N.E.C. | 9SALMONELLA | Florida District Office (FLA-DO) |
| 10/4/2011 | 28FGT04CURRY POWDER, GROUND, CRACKED, WITHOUT SALT | 9SALMONELLA | Florida District Office (FLA-DO) |
| 10/4/2011 | 28FGT04CURRY POWDER, GROUND, CRACKED, WITHOUT SALT | 9SALMONELLA | Florida District Office (FLA-DO) |
| 8/24/2011 | 28FAH04CURRY POWDER, GROUND, CRACKED, WITHOUT SALT | 9SALMONELLA | New York District Office (NYK-DO) |
| 4/8/2008 | 28EGT04CURRY POWDER, WITHOUT SALT | 9SALMONELLA | Florida District Office (FLA-DO) |
| 5/7/2007 | 28FGT04CURRY POWDER, GROUND, CRACKED, WITHOUT SALT | 9SALMONELLA | Florida District Office (FLA-DO) |
| 2/6/2007 | 28EGT04CURRY POWDER, WITHOUT SALT | 9SALMONELLA | Florida District Office (FLA-DO) |
| 1/16/2007 | 28FCT04CURRY POWDER, GROUND, CRACKED, WITHOUT SALT | 9SALMONELLA | Division of Southeast Imports (DSEI) |
| 11/16/2004 | 28FGT04CURRY POWDER, GROUND, CRACKED, WITHOUT SALT | 9SALMONELLA | New York District Office (NYK-DO) |
Frequently Asked Questions
What is BETAPAC MANUFACTURER COMPANY LIMITED's FDA import refusal history?
BETAPAC MANUFACTURER COMPANY LIMITED (FEI: 3014100495) has 26 FDA import refusal record(s) in our database, spanning from 11/16/2004 to 12/3/2025.
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. BETAPAC MANUFACTURER COMPANY LIMITED's FEI number is 3014100495.
What types of violations has BETAPAC MANUFACTURER COMPANY LIMITED received?
BETAPAC MANUFACTURER COMPANY LIMITED 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 BETAPAC MANUFACTURER COMPANY LIMITED come from?
All FDA import refusal data for BETAPAC MANUFACTURER COMPANY LIMITED 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.