Magnegita
Recall
|
Medicines
|
24/05/2013
The marketing authorization holder has informed its supplied customers in a letter dated 24.05.2013 that particles were observed in some vials. For this reason, the above mentioned batches are recalled as a precautionary measure.
| Name of the medicinal product | Magnegita 500 Mikromol/ml Injektionslösung |
|---|---|
| Marketing authorisation number(s) | AT-Zulassungsnummer: 1-27303 DE-Zulassungsnummer: 65896.00.00 |
| Marketing authorisation holder | Agfa Healthcare Imaging Agents GmbH Am Coloneum 4 DE-50829 Köln |
| Batch number(s) | AT-Zulassungsnummer 1-27303: 181211/2AT, 201010/2AT, 50710/4AT, 160910/4AT, 40710B4AT, 60311/5AT, 181211/6AT, 100709/2AT, 50710/4AT DE-Zulassungsnummer 65896.00.00: 281110/2DE, 110810/6DE, 120810/6DE, 231010/6DE, 281110/6DE, 311110/6DE, , 191010/4DE, 80711/6DE, 141211/4DE,171211/2DE, 50710A4DE, 100811/6DE, 100709/2DE, 150809B4DE |
| Classification of the recall | 2 |
| BASG reference number | INS-640.001-0767 |
Further inquiry note
Page last modified:
12/07/2022