Zoledronic Acid
Recall
|
Medicines
|
17/06/2014
The marketing authorization holder informed its supplied customers in a letter dated June 16, 2014, that the manufacturer cannot rule out the possibility that the solution in individual bottles is contaminated with small black particles, so that a precautionary recall has been initiated.
Name of the medicinal product | Zoledronsäure Genericon 4 mg/100 ml Infusionslösung |
---|---|
Marketing authorisation number(s) | 135130 |
Marketing authorisation holder | Genericon Pharma GmbH |
Batch number(s) | 5001271 |
Classification of the recall | 2 |
BASG reference number | INS - 640.001 - 1 039 |
Further inquiry note
Page last modified:
12/07/2022