Calcium "Fresenius"-Ampullen
Replacement
|
Medicines
|
06/06/2011
The marketing authorization holder informed its supplied customers by letter dated 06.06.2011 that a precautionary recall is being carried out due to three reports of crystallization of the calcium solution.
| Name of the medicinal product | Calcium "Fresenius" - Ampullen |
|---|---|
| Marketing authorisation number(s) | 1-18323 |
| Marketing authorisation holder | Fresenius Kabi Austria GmbH |
| Batch number(s) | L108003, L118002 |
| Classification of the recall | 2 |
| BASG reference number | INS-640.001-0123 |
Further inquiry note
Page last modified:
12/07/2022