EU + POLAND EVIDENCE PROFILE

Mucuna pruriens EU Novel Food status & enforcement 2026

A botanical where the non-binding EU status signal and the 2026 Dutch product recalls must be recorded as different evidence types, then checked across direct ingredients and blends.

STATUSACTIVE NL RECALL CLUSTER
JURISDICTIONEuropean Union · Netherlands · Poland
RULE VERSIONSV-ING-MUC-2026.09.19
LAST CHECKED2026-09-19
01

IDENTITY BEFORE STATUS

Name, part and form

Name
Mucuna pruriens
Synonyms
Velvet bean · fluweelboon · Mucuna seed extract · L-Dopa botanical
Botanical / chemical identity
Mucuna pruriens (L.) DC.
Plant part
Seed in the reviewed RIVM assessment; confirm any other plant part independently.
Reviewed form
Seed and seed extracts, including extracts standardised for levodopa (L-Dopa); exact form, DER, solvent and assay remain product-specific.
02

CLAIMS

What the profile supports

NO AUTHORISED CLAIM ASSERTED
  • Do not infer a permitted health claim from traditional use or botanical wording.
  • Memory, mood, energy, fertility, dopamine and Parkinson-related wording require separate claims and medicinal-presentation review.

This page does not identify a product-ready authorised EU health claim for Mucuna pruriens or levodopa.

03

RESTRICTIONS

Conditions that can change the answer

  1. 01

    Resolve the exact ingredient identity in every formula and blend; a product name may not disclose that Mucuna is present.

  2. 02

    Treat the Novel Food Catalogue as orientation only. Verify Union-list status, any applicant-specific route, national interpretation and the actual recall notice before a legal or operational decision.

  3. 03

    The RIVM safety assessment reports that a safe dose could not be established from the available public evidence and provides precautionary advice for defined groups.

  4. 04

    A Dutch recall notice does not automatically establish the same enforcement action, scope or deadline in another EU market.

04

STATUS → ENFORCEMENT → RECALLS

Evidence timeline

RISK ASSESSMENT

RIVM publishes Mucuna pruriens safety advice

Safety context is added to the evidence ledger. It is not represented as a 2026 recall decision.

Open source ↗
RECALL EVENT

Dutch product notices begin listing Mucuna products

Distributor records name multiple direct-ingredient products and state an all-batch scope for the listed EANs.

Open source ↗
RECALL EVENT

Multi-ingredient products appear in the cluster

Retailer notices include Ortho Multi Man, showing why formula-level identity resolution must go beyond the product title.

Open source ↗
REGULATORY CONTEXT

Status and enforcement remain separate

Suppvera records the Commission Catalogue as non-binding context and the named notices as event evidence; neither automatically creates an EU-wide stop-sale decision.

Open source ↗

A status interpretation and a product recall are stored as different evidence classes. This timeline does not create an EU-wide prohibition or execute a stop-sale action.

05

POLISH NOTES

National regulatory layer

For Poland, perform a separate product-level Novel Food, ingredient, medicinal-presentation, claims and notification review; the Dutch notices are evidence of enforcement activity, not a Polish decision.

Keep supplier specification, plant part, extraction, L-Dopa assay, daily portion and blend composition linked to the exact SKU and batch.

06

PRIMARY SOURCES

Evidence ledger

SRC-01
European Commission

Novel Food status Catalogue

Status orientation only; non-exhaustive and not recall evidence

RULE / SOURCE VERSIONLive non-binding catalogue, checked 19 September 2026Open primary source ↗
SRC-02
RIVM

Risk assessment of herbal preparations containing Mucuna pruriens seed extracts

Seed-extract safety context and uncertainty

RULE / SOURCE VERSIONRIVM report 2024-0087Open primary source ↗
SRC-03
Superfoodstore

Safety warnings and Mucuna pruriens recall list

Named products, EANs and all-batch recall scope

RULE / SOURCE VERSIONDistributor notices dated 24–31 August 2026, checked 19 September 2026Open primary source ↗
SRC-04
Vitatheek

Recall and product-withdrawal notices

Direct and multi-ingredient products including Ortho Multi Man

RULE / SOURCE VERSIONRetailer notices checked 19 September 2026Open primary source ↗

Apply the evidence to your wording.

Check your product ↗