Maisonneuve
⚠️ Moderate Risk
FEI: 3002937221 • Montreal, QC • CANADA
FEI Number
3002937221
Location
Montreal, QC
Country
CANADAAddress
4445 Rue Ontario Est, , Montreal, QC, Canada
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
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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.
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.
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).
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
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.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/23/2002 | 29BEY60SODA WATER, CARBONATED | 473LABELING | New York District Office (NYK-DO) |
| 10/23/2002 | 27YCE06PEPPER SAUCE (HOT, MILD, ETC.) | New York District Office (NYK-DO) | |
| 10/23/2002 | 03MGT02CHOCOLATE COOKIE, BISCUIT, WAFER DOUGH | New York District Office (NYK-DO) | |
| 10/23/2002 | 33LHE02CARAMEL CANDY PIECES, SOFT, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE) | 11UNSAFE COL | New York District Office (NYK-DO) |
| 9/30/2002 | 35AFY01GELATIN, FLAVORED | 473LABELING | New York District Office (NYK-DO) |
| 9/30/2002 | 38AFH29VEGETABLE (SINGLE INGREDIENT NOT MENTIONED ELSEWHERE) SOUP | 473LABELING | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Maisonneuve's FDA import refusal history?
Maisonneuve (FEI: 3002937221) has 6 FDA import refusal record(s) in our database, spanning from 9/30/2002 to 10/23/2002.
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. Maisonneuve's FEI number is 3002937221.
What types of violations has Maisonneuve received?
Maisonneuve has been cited for 8 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 Maisonneuve come from?
All FDA import refusal data for Maisonneuve 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.