Buerlecithin
Recall
|
Medicines
|
05/07/2017
The marketing authorization holder has informed its supplied customers in a letter dated July 04, 2017, that individual bottles filled with distilled water were included in the packaging of Buerlecithin liquid 500 ml. For this reason, this batch is recalled. There is no risk to patient safety.
| Name of the medicinal product | Buerlecithin flüssig |
|---|---|
| Marketing authorisation number(s) | HERB-00042 |
| Marketing authorisation holder | Takeda Pharma Ges.m.b.H. |
| Batch number(s) | 350131 |
| Classification of the recall | 3 |
| BASG reference number | INS-640.001-2175 |
Further inquiry note
Page last modified:
12/07/2022