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Tumenta Mary

⚠️ Moderate Risk

FEI: 3010131077 • Yaounde • CAMEROON

FEI

FEI Number

3010131077

📍

Location

Yaounde

🇨🇲

Country

CAMEROON
🏢

Address

Yaounde, , Yaounde, , Cameroon

Moderate Risk

FDA Import Risk Assessment

32.8
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

8
Total Refusals
9
Unique Violations
8/26/2015
Latest Refusal
8/6/2013
Earliest Refusal

Score Breakdown

Violation Severity
45.8×40%
Refusal Volume
35.3×30%
Recency
0.0×20%
Frequency
38.9×10%
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

2186×

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.

3216×

LACKS N/C

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)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

3286×

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.

115×

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).

3205×

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.

4825×

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.

2491×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

641×

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.

3241×

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)).

Refusal History

DateProductViolationsDivision
8/26/2015
38MHT99BROTH, N.E.C. (MEAT AND/OR VEGETABLE STOCK)
218LIST INGRE
320LACKS FIRM
321LACKS N/C
328USUAL NAME
482NUTRIT LBL
Baltimore District Office (BLT-DO)
8/26/2015
29AGT99NONCARBONATED SOFT DRINK, N.E.C.
218LIST INGRE
320LACKS FIRM
321LACKS N/C
328USUAL NAME
482NUTRIT LBL
Baltimore District Office (BLT-DO)
8/26/2015
29AGT99NONCARBONATED SOFT DRINK, N.E.C.
11UNSAFE COL
218LIST INGRE
321LACKS N/C
328USUAL NAME
482NUTRIT LBL
Baltimore District Office (BLT-DO)
8/26/2015
29AGT99NONCARBONATED SOFT DRINK, N.E.C.
11UNSAFE COL
218LIST INGRE
320LACKS FIRM
321LACKS N/C
328USUAL NAME
482NUTRIT LBL
Baltimore District Office (BLT-DO)
8/26/2015
29AGT99NONCARBONATED SOFT DRINK, N.E.C.
11UNSAFE COL
218LIST INGRE
320LACKS FIRM
321LACKS N/C
324NO ENGLISH
328USUAL NAME
482NUTRIT LBL
Baltimore District Office (BLT-DO)
8/26/2015
29AGT99NONCARBONATED SOFT DRINK, N.E.C.
11UNSAFE COL
64YELLOW #5
Baltimore District Office (BLT-DO)
8/26/2015
29AGT99NONCARBONATED SOFT DRINK, N.E.C.
11UNSAFE COL
Baltimore District Office (BLT-DO)
8/6/2013
16AGH99FISH, N.E.C.
218LIST INGRE
249FILTHY
320LACKS FIRM
321LACKS N/C
328USUAL NAME
Baltimore District Office (BLT-DO)

Frequently Asked Questions

What is Tumenta Mary's FDA import refusal history?

Tumenta Mary (FEI: 3010131077) has 8 FDA import refusal record(s) in our database, spanning from 8/6/2013 to 8/26/2015.

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. Tumenta Mary's FEI number is 3010131077.

What types of violations has Tumenta Mary received?

Tumenta Mary has been cited for 9 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 Tumenta Mary come from?

All FDA import refusal data for Tumenta Mary 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.