Distribuidora La Casa Grande
⚠️ Moderate Risk
FEI: 3003967495 • N.L.Mexico. • MEXICO
FEI Number
3003967495
Location
N.L.Mexico.
Country
MEXICOAddress
Central 303 Norte, , San Pedro,Santiago,N.L.Mexico., , 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
YELLOW #5
The food appears to bear or contain the color additive FD & C Yellow No. 5, which is not declared on the label per 21 CFR 74.705(a)(c) under section 721.
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).
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
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.
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.
PESTICIDES
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:
ADDED BULK
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the food appears to have a substance added to, mixed or packed with it so as to increase its bulk or weight, or reduce its quality or strength, or make it appear better or of greater value than it is.
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.
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.
ALLERGEN
the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).
TRANSFAT
The product is misbranded under Section 403(q) because the nutrition label does not provide all of the information required by 21 CFR 101.9(c); specifically, the label does not bear the amount of trans fat [21 CFR 101.9(c)(2)(ii)].
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.
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.
SUBSTITUTE
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears that a substance has been substituted wholly or in part for one or more of the article's ingredients.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/18/2009 | 16AGH99FISH, N.E.C. | 9SALMONELLA | Southwest Import District Office (SWI-DO) |
| 1/20/2009 | 07BGT02CORN CHIPS, FRIED | Southwest Import District Office (SWI-DO) | |
| 12/18/2008 | 33AGT02CARAMEL CANDY PIECES, HARD, WITH NUTS OR NUT PRODUCTS (NOT COCONUT) (WITHOUT CHOCOLATE) | Southwest Import District Office (SWI-DO) | |
| 11/19/2008 | 16AGT99FISH, N.E.C. | 9SALMONELLA | Southwest Import District Office (SWI-DO) |
| 2/29/2008 | 36CCT01COMB HONEY | Southwest Import District Office (SWI-DO) | |
| 11/13/2007 | 16AGH99FISH, N.E.C. | 2920PESTICIDES | Southwest Import District Office (SWI-DO) |
| 11/13/2007 | 33HGT05CANDY BAR OR PIECES (NOT CARAMEL OR FONDANT), SOFT, WITH COCONUT (WITHOUT CHOCOLATE) | 64YELLOW #5 | Southwest Import District Office (SWI-DO) |
| 9/12/2007 | 33JGT02CARAMEL CANDY PIECES, SOFT, WITH FRUIT (WITHOUT CHOCOLATE) | 64YELLOW #5 | Southwest Import District Office (SWI-DO) |
| 7/5/2007 | 33HGT05CANDY BAR OR PIECES (NOT CARAMEL OR FONDANT), SOFT, WITH COCONUT (WITHOUT CHOCOLATE) | Southwest Import District Office (SWI-DO) | |
| 4/16/2007 | 33HGT05CANDY BAR OR PIECES (NOT CARAMEL OR FONDANT), SOFT, WITH COCONUT (WITHOUT CHOCOLATE) | 64YELLOW #5 | Southwest Import District Office (SWI-DO) |
| 4/3/2007 | 33HGT05CANDY BAR OR PIECES (NOT CARAMEL OR FONDANT), SOFT, WITH COCONUT (WITHOUT CHOCOLATE) | 64YELLOW #5 | Southwest Import District Office (SWI-DO) |
| 12/4/2006 | 36CCT04HONEY | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is Distribuidora La Casa Grande's FDA import refusal history?
Distribuidora La Casa Grande (FEI: 3003967495) has 12 FDA import refusal record(s) in our database, spanning from 12/4/2006 to 12/18/2009.
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. Distribuidora La Casa Grande's FEI number is 3003967495.
What types of violations has Distribuidora La Casa Grande received?
Distribuidora La Casa Grande has been cited for 14 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 Distribuidora La Casa Grande come from?
All FDA import refusal data for Distribuidora La Casa Grande 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.