Recall | Medicines | 29/06/2012

The marketing authorization holder informed its supplied customers by letter dated 28.06.2012 that the transport carton of batch A010816 is labeled with the strength "Propofol ratiopharm 10 mg/ml emulsion for injection or infusion" (500 mg/50 ml), but there are 10 packages with the strength "Propofol ratiopharm 20 mg/ml Emulsion for Injection or Infusion" (1000 mg/50 ml) inside.

Name of the medicinal product 1. Propofol ratiopharm 10 mg/ml Emulsion zur Injektion oder Infusion
2. Propofol ratiopharm 20 mg/ml Emulsion zur Injektion oder Infusion
Marketing authorisation number(s) 1. 1-30747
2. 1-30748
Marketing authorisation holder ratiopharm Arzneimittel Vertriebs GmbH
Batch number(s) A010816
Classification of the recall1
BASG reference number INS-640.001-0473

Further inquiry note