Octagam 50 mg/ml
Replacement
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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 |
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Marketing authorisation number(s) | 2-00169 |
Marketing authorisation holder | Octapharma Pharmazeutika Produktionsges.m.b.H |
Batch number(s) | C340A8481 |
Classification of the recall | 2 |
BASG reference number | INS-640.001-0965 |
Further inquiry note
Page last modified:
12/07/2022