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 recall2
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