Propofol
Recall
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Medicines
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17/11/2015
The marketing authorization holder has informed its supplied customers in a letter dated 17.11.2015 that the above mentioned batch has a blue instead of green "flip-off" cap. To avoid confusion with "Propofol ratiopharm 10 mg/ml Emulsion for Injection/Infusion" (blue cap), batch A050007 is recalled as a precaution.
Name of the medicinal product | Propofol ratiopharm 20 mg/ml Emulsion zur Injektion oder Infusion |
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Marketing authorisation number(s) | 1-30748 |
Marketing authorisation holder | ratiopharm Arzneimittel Vertriebs-GmbH |
Batch number(s) | A050007 |
Classification of the recall | 2 |
BASG reference number | INS - 640.001 - 1 559 |
Further inquiry note
Page last modified:
12/07/2022