Recall | Medicines | 26/01/2011

The marketing authorization holder has informed its supplied customers in a letter dated January 25, 2011, that cracks have been detected in the cone of some prefilled syringes. At present, there is no indication that sterility is impaired by this defect, but the above batch is nevertheless being recalled as a precautionary measure.

Name of the medicinal product Pegasys 180 Mikrogramm Injektionslösung in einer Fertigspritze
Marketing authorisation number(s) EU/1/02/221/008
Marketing authorisation holder Roche Registration Ltd.

Durchführung Rückruf:
Roche Austria GmbH
Batch number(s) B1208B01
Classification of the recall1
BASG reference number INS-640.001-0013

Further inquiry note