Dancor
Recall
|
Medicines
|
17/09/2013
The marketing authorization holder has informed its supplied customers in a letter dated 13.09.2013 that investigations have shown that the optimal efficacy of batch 15159721 cannot be guaranteed over the entire shelf life and therefore a precautionary recall of the affected batch is being carried out. All other batches of Dancor available in Austria are not affected by this recall.
| Name of the medicinal product | Dancor 10 mg - Tabletten |
|---|---|
| Marketing authorisation number(s) | 1-20773 |
| Marketing authorisation holder | Merck GmbH |
| Batch number(s) | 15159721 |
| Classification of the recall | 2 |
| BASG reference number | INS -640.001 -0897 |
Further inquiry note
Page last modified:
12/07/2022