Tardocillin
Recall
|
Medicines
|
09/10/2013
On October 8, 2013, the marketing authorization holder informed its customers that injection vials may have an externally invisible defect under the crimp cap due to the capping machine and that product leakage may occur when the vial is shaken. Since sterility cannot be guaranteed, this batch is being recalled. This medicinal product is authorized in Germany and is placed on the market in Austria within the scope of a transfer notification according to the Medicinal Products Import Act 2010.
| Name of the medicinal product | Tardocillin 1200 |
|---|---|
| Marketing authorisation number(s) | Zul.-Nr. Deutschland: 6070615.00.00 |
| Marketing authorisation holder | INFECTOPHARM Arzneimittel und Consilium GmbH |
| Batch number(s) | A0113011 |
| Classification of the recall | 2 |
| BASG reference number | INS-640.001-0917 |
Further inquiry note
Page last modified:
12/07/2022