Pegasys
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 recall | 1 |
| BASG reference number | INS-640.001-0013 |
Further inquiry note
Page last modified:
12/07/2022