Cobactan
Recall
|
Medicines
|
27/08/2015
The marketing authorization holder informed its supplied customers in a letter dated August 25, 2015, that a different number of small particles was observed in some bottles of the above-mentioned batches after preparation of the ready-to-use solution. Thus, the result is out of specification with regard to the test "Description after preparation of the ready-to-use solution", which results in a precautionary recall of the three batches.
| Name of the medicinal product | Cobactan 4,5 % w/v Pulver und Lösungsmittel zur Herstellung einer Injektionslösung für Pferde und Rinder |
|---|---|
| Marketing authorisation number(s) | 8-00667 |
| Marketing authorisation holder | Intervet GmbH Durchführung Rückruf: Intervet Deutschland GmbH |
| Batch number(s) | A129A01 A129A02 A130A01 |
| Classification of the recall | 2 |
| BASG reference number | INS-640.001-1483 |
Further inquiry note
Page last modified:
12/07/2022