BioMonde BioBag
Recall
|
Medicines
|
25/02/2014
The distributor informed its supplied customers on 03.01.2014 that during the daily control of the sterility tests of the final products of batch 02-140102 a turbidity was detected and therefore a potential contamination had to be assumed.
| Name of the medicinal product | 1 .BioMonde BioBag 50 2. BioMonde BioBag 200 (Es handelt sich bei diesen Produkten um Larven der Art Lucilia sericata) |
|---|---|
| Marketing authorisation number(s) | Keine (Arzneimittel gemäß § 7 Abs 6d Arzneimittelgesetz idgF.) |
| Marketing authorisation holder | Hersteller: BioMonde GmbH, Deutschland Vertrieb: sorbion mayrhofer gmbh, Österreich |
| Batch number(s) | 02-140102 |
| Classification of the recall | 2 |
| BASG reference number | INS-640.001-1021 |
Further inquiry note
Page last modified:
12/07/2022