Robinul
Recall
|
Medicines
|
16/08/2018
The marketing authorization holder informed its supplied customers in a letter dated August 16, 2018, that due to quality problems with one batch of ampoules, batch D1K13 is being recalled as a precautionary measure.
Name of the medicinal product | Robinul 0,2 mg - Ampullen |
---|---|
Marketing authorisation number(s) | 1-18081 |
Marketing authorisation holder | Chiesi Pharmaceuticals GmbH |
Batch number(s) | D1K13 |
Classification of the recall | 1 |
BASG reference number | INS-640.001-2611 |
Further inquiry note
Page last modified:
12/07/2022