Braunoderm
Recall
|
Medicines
|
26/05/2011
The marketing authorization holder informed its supplied customers in a letter dated May 20, 2011, that the content of available iodine in the three batches listed above may fall slightly below the specification limit before expiry of the shelf life and that a recall therefore had to be carried out.
| Name of the medicinal product | Braunoderm |
|---|---|
| Marketing authorisation number(s) | Zulassungs-Nr. Deutschland: 6726033.00.00 |
| Marketing authorisation holder | B. Braun Melsungen AG Carl-Braun-Str. 1, 34212 Melsungen, Deutschland |
| Batch number(s) | 0103M11, 0183M14, 0253M14 |
| Classification of the recall | 2 |
| BASG reference number | INS-640.001-0134 (Dieser Rückruf wurde ohne vorherige/gleichzeitige Meldung an das Bundesamt für Sicherheit im Gesundheitswesen bekannt gemacht) |
Further inquiry note
Page last modified:
12/07/2022