Joannusmolen
FDA import alert and refusal historyCuijk, NetherlandsFEI 3014216118
Recorded by FDA as JOANNUSMOLEN
As of October 26, 2026, Joannusmolen (Cuijk, Netherlands) is on the red list of FDA Import Alert 40-05 (Adulterated and misbranded infant formula) for ekobaby zuigelingenmelk 1; ekobaby groeimelk 3; ekobaby opvolgmelk 2, published by FDA on September 20, 2018, and has 3 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
- Milk base infant formula product (0-12 months), powder formula · NO ENGLISH
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Joannusmolen
4 records, newest first. Each line links to the FDA page it came from.
2018
- Import alert listingListed on Import Alert 40-05red listEkoBaby Zuigelingenmelk 1; EkoBaby Groeimelk 3; EkoBaby Opvolgmelk 2Source
- Import refusalSource
Refused, 3 lines in one entry: Milk base infant formula product (0-12 months), powder formulaNO ENGLISHEntry 660-2532230-7Show 3 linesHide lines
- Refused, Milk base infant formula product (0-12 months), powder formulaNO ENGLISHEntry 660-2532230-7Source
- Refused, Milk base infant formula product (0-12 months), powder formulaNO ENGLISHEntry 660-2532230-7Source
- Refused, Milk base infant formula product (0-12 months), powder formulaNO ENGLISHEntry 660-2532230-7Source
Refusal charges, in plain English
- NO ENGLISH3 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.
Questions about Joannusmolen
- Is Joannusmolen on an FDA import alert?
- Yes. As of October 26, 2026, Joannusmolen is on the red list of FDA Import Alert 40-05, “Adulterated and misbranded infant formula”, for ekobaby zuigelingenmelk 1; ekobaby groeimelk 3; ekobaby opvolgmelk 2; FDA published the listing on September 20, 2018.
- Has FDA refused shipments from Joannusmolen?
- Yes. FDA refused 3 shipment lines from Joannusmolen on June 18, 2018. The most recent, on June 18, 2018, was milk base infant formula product (0-12 months), powder formula, charged as NO ENGLISH (required label information not in english).
- Why did FDA refuse Joannusmolen's shipments?
- The most frequent charge is NO ENGLISH (required label information not in english, 3 lines).
- What is Joannusmolen's FEI number?
- Joannusmolen's FDA Establishment Identifier (FEI) is 3014216118.
- Can shipments from Joannusmolen still enter the U.S.?
- Shipments of ekobaby zuigelingenmelk 1; ekobaby groeimelk 3; ekobaby opvolgmelk 2 from Joannusmolen 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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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.