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Potentia Trium B.V

⚠️ Moderate Risk

FEI: 3017103463 • Rotterdam, Zuid-Holland • NETHERLANDS

FEI

FEI Number

3017103463

📍

Location

Rotterdam, Zuid-Holland

🇳🇱
🏢

Address

Corkstraat 46, , Rotterdam, Zuid-Holland, Netherlands

Moderate Risk

FDA Import Risk Assessment

46.5
LowModerateHighCritical

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

Statistics

15
Total Refusals
11
Unique Violations
4/29/2022
Latest Refusal
1/22/2021
Earliest Refusal

Score Breakdown

Violation Severity
44.8×40%
Refusal Volume
44.6×30%
Recency
25.9×20%
Frequency
100.0×10%
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

4829×

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.

3246×

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)).

3214×

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.

21603×

LACK NOTIF

Adulterated, 801(a)(3), lack of documentation establishing that the infant formula meets all notification conditions required by 412(c) or 412(d), Prohibited Act, Section 301(s).

3203×

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.

2601×

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.

33201×

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)].

33611×

NUTR DEF

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the infant formula appears to adulterated in that it does not provide the nutrients required by 21 CFR 107.100

2181×

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.

621×

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).

831×

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

DateProductViolationsDivision
4/29/2022
40PGT99OTHER FORMULA PRODUCTS, N.E.C., POWDER FORMULA
260FALSE
3361NUTR DEF
Division of Northern Border Imports (DNBI)
12/30/2021
21FYT09OTHER FRUITS, MIXED FRUIT PUREES
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
Division of Southeast Imports (DSEI)
12/21/2021
21FYT09OTHER FRUITS, MIXED FRUIT PUREES
3320TRANSFAT
482NUTRIT LBL
Division of Southeast Imports (DSEI)
10/28/2021
40PYY01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), POWDER FORMULA
320LACKS FIRM
321LACKS N/C
482NUTRIT LBL
Division of Southeast Imports (DSEI)
10/13/2021
40PET01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), POWDER FORMULA
2160LACK NOTIF
482NUTRIT LBL
Division of Southeast Imports (DSEI)
9/29/2021
40PFT99OTHER FORMULA PRODUCTS, N.E.C., POWDER FORMULA
2160LACK NOTIF
482NUTRIT LBL
Division of Southeast Imports (DSEI)
9/29/2021
40PFT99OTHER FORMULA PRODUCTS, N.E.C., POWDER FORMULA
2160LACK NOTIF
482NUTRIT LBL
Division of Southeast Imports (DSEI)
7/21/2021
40NET01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), READY TO FEED
218LIST INGRE
321LACKS N/C
482NUTRIT LBL
Division of Northern Border Imports (DNBI)
6/15/2021
40PET01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), POWDER FORMULA
320LACKS FIRM
321LACKS N/C
482NUTRIT LBL
Division of Northern Border Imports (DNBI)
5/17/2021
40NFT01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), READY TO FEED
320LACKS FIRM
321LACKS N/C
324NO ENGLISH
482NUTRIT LBL
Division of Northern Border Imports (DNBI)
3/3/2021
40NFT01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), READY TO FEED
324NO ENGLISH
Division of West Coast Imports (DWCI)
2/12/2021
40NVT01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), READY TO FEED
324NO ENGLISH
Division of West Coast Imports (DWCI)
2/12/2021
40NVT01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), READY TO FEED
324NO ENGLISH
Division of West Coast Imports (DWCI)
2/12/2021
40NET01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), READY TO FEED
324NO ENGLISH
Division of West Coast Imports (DWCI)
1/22/2021
40NVT01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), READY TO FEED
324NO ENGLISH
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is Potentia Trium B.V's FDA import refusal history?

Potentia Trium B.V (FEI: 3017103463) has 15 FDA import refusal record(s) in our database, spanning from 1/22/2021 to 4/29/2022.

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. Potentia Trium B.V's FEI number is 3017103463.

What types of violations has Potentia Trium B.V received?

Potentia Trium B.V has been cited for 11 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 Potentia Trium B.V come from?

All FDA import refusal data for Potentia Trium B.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.