Cardiolite/Neurolite
Recall
|
Medicines
|
30/08/2011
The distribution company has informed its supplied customers by letter dated August 29, 2011, that the batches indicated above may be contaminated with particles and are therefore recalled as a precautionary measure.
| Name of the medicinal product | Cardiolite – Trockenstechampullen Neurolite 99mTechnetiumbicisat-Injektion - Kit für ein radioaktives Arzneimittel |
|---|---|
| Marketing authorisation number(s) | Cardiolite: 4-00001 Neurolite: 4-00002 |
| Marketing authorisation holder | Lantheus MI UK Ltd Festival House 39 Oxford Street, Newbury Berkshire, RG14 1JG, GB Vertrieb und Durchführung Rückruf: THP MEDICAL PRODUCTS Vertriebs GmbH |
| Batch number(s) | Cardiolite: 4000BE, 4026BE Neurolite: A5127AE.B5605AE, A5127AE1.B5605AE1 |
| Classification of the recall | 2 |
| BASG reference number | INS-640.001-0216 |
Further inquiry note
Page last modified:
12/07/2022