Octagam 50 mg/ml

Replacement | Medicines | 30/12/2013

The marketing authorization holder informed its supplied customers in a letter dated December 23, 2013, that it cannot be ruled out that a frequent occurrence of hypersensitivity reactions may occur with this batch and that a precautionary withdrawal from the market is therefore being carried out.

Name of the medicinal product Octagam 50 mg/ml Infusionslösung
Marketing authorisation number(s) 2-00169
Marketing authorisation holder Octapharma Pharmazeutika Produktionsges.m.b.H
Batch number(s) C340A8481
Classification of the recall2
BASG reference number INS-640.001-0965
Email

Further inquiry note