The following is punishable by a fifth-class fine:
1° For a healthcare establishment, an interhospital syndicate, a health cooperation grouping using in vitro diagnostic medical devices or a blood transfusion establishment mentioned in article R. 5222-10, not to appoint a reactovigilance correspondent or not to communicate the name of this correspondent to the Director General of the Agence nationale de sécurité du médicament et des produits de santé ;
2° For a healthcare professional who is aware of a failure or alteration of an in vitro diagnostic medical device likely to have harmful effects on the health of individuals, to refrain from reporting this immediately to the Agence nationale de sécurité du médicament et des produits de santé.