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 recall3
BASG reference number INS-640.001-2175

Further inquiry note