Potentia Trium B.V
FDA import alert and refusal historyRotterdam, NetherlandsFEI 3017103463
As of October 25, 2026, Potentia Trium B.V (Rotterdam, Netherlands) is on the red list of FDA Import Alert 40-05 (Adulterated and misbranded infant formula) for loulouka goat follow-on formula, published by FDA on November 15, 2021, and has 15 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 40-05 · red list
- Last import refusal
- Other formula products, n.e.c., powder formula · FALSE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Potentia Trium B.V
16 records, newest first. Each line links to the FDA page it came from.
2022
- Import refusalSource
2021
- Import refusalRefused, Other fruits, mixed fruit pureesNUTRIT LBLNEEDS FCENO PROCESSEntry SCS-9226382-3Source
- Import refusalRefused, Other fruits, mixed fruit pureesTRANSFATNUTRIT LBLEntry SCS-8989002-6Source
- Import alert listingListed on Import Alert 40-05red listLoulouka Goat Follow-On FormulaSource
- Import refusalRefused, Milk base infant formula product (0-12 months), powder formulaLACKS FIRMLACKS N/CNUTRIT LBLEntry AEK-9532502-0Source
- Import refusalRefused, Milk base infant formula product (0-12 months), powder formulaLACK NOTIFNUTRIT LBLEntry 799-5362294-0Source
- Import refusalRefused, Other formula products, n.e.c., powder formulaLACK NOTIFNUTRIT LBLEntry AEK-9535322-0Source
- Import refusalRefused, Other formula products, n.e.c., powder formulaLACK NOTIFNUTRIT LBLEntry AEK-9535432-7Source
- Import refusalRefused, Milk base infant formula product (0-12 months), ready to feedLIST INGRELACKS N/CNUTRIT LBLEntry AEK-8914601-0Source
- Import refusalRefused, Milk base infant formula product (0-12 months), powder formulaLACKS FIRMLACKS N/CNUTRIT LBLEntry AEK-9217425-6Source
- Import refusalRefused, Milk base infant formula product (0-12 months), ready to feedLACKS FIRMLACKS N/CNO ENGLISHNUTRIT LBLEntry AEK-9076956-0Source
- Import refusalRefused, Milk base infant formula product (0-12 months), ready to feedNO ENGLISHEntry AEK-8670246-8Source
- Import refusalRefused, Milk base infant formula product (0-12 months), ready to feedNO ENGLISHEntry AEK-8664525-3Source
- Import refusalRefused, Milk base infant formula product (0-12 months), ready to feedNO ENGLISHEntry AEK-8658916-2Source
- Import refusalRefused, Milk base infant formula product (0-12 months), ready to feedNO ENGLISHEntry AEK-8664508-9Source
Show 1 earlier record (2021)Hide earlier records
2021
- Import refusalRefused, Milk base infant formula product (0-12 months), ready to feedNO ENGLISHEntry AEK-8656961-0Source
Refusal charges, in plain English
- NUTRIT LBL9 refused lines
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
- NO ENGLISH6 refused lines
Required label information not in English
Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.
- LACKS N/C4 refused lines
Net quantity statement missing
The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.
- LACK NOTIF3 refused lines
LACK NOTIF
- LACKS FIRM3 refused lines
Manufacturer name and address missing
The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.
- FALSE1 refused line
False or misleading labeling
The labeling appeared to be false or misleading in some particular.
- LIST INGRE1 refused line
Ingredients not listed
The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).
- NEEDS FCE1 refused line
Processor not registered for canned or acidified foods
The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.
Questions about Potentia Trium B.V
- Is Potentia Trium B.V on an FDA import alert?
- Yes. As of October 25, 2026, Potentia Trium B.V is on the red list of FDA Import Alert 40-05, “Adulterated and misbranded infant formula”, for loulouka goat follow-on formula; FDA published the listing on November 15, 2021.
- Has FDA refused shipments from Potentia Trium B.V?
- Yes. FDA refused 15 shipment lines from Potentia Trium B.V between January 22, 2021 and April 29, 2022. The most recent, on April 29, 2022, was other formula products, n.e.c., powder formula, charged as FALSE (false or misleading labeling).
- Why did FDA refuse Potentia Trium B.V's shipments?
- The most frequent charges are NUTRIT LBL (nutrition information missing from label, 9 lines) and NO ENGLISH (required label information not in english, 6 lines).
- What is Potentia Trium B.V's FEI number?
- Potentia Trium B.V's FDA Establishment Identifier (FEI) is 3017103463.
- Can shipments from Potentia Trium B.V still enter the U.S.?
- Shipments of loulouka goat follow-on formula from Potentia Trium B.V can be detained without physical examination under Import Alert 40-05; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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