Propofol
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 recall | 1 |
| BASG reference number | INS-640.001-0473 |
Further inquiry note
Page last modified:
12/07/2022