Peritrast - Lösung zur parenteralen Anwendung
Recall
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Medicines
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12/07/2024
The marketing authorisation holder informed its customers on July 12, 2024 that visible particles in solution were detected during stability tests. For this reason, the mentioned batches are being recalled as a precautionary measure.
| Name of the medicinal product | 1. Peritrast 300 mg Jod/ml - Lösung zur parenteralen Anwendung 2. Peritrast 180 mg Jod/ml - Lösung zur parenteralen Anwendung |
|---|---|
| Marketing authorisation number(s) | 1. 1-24112 2. 1-24113 |
| CIP code | 1. 3263496 2. 2802502, 2802519 |
| Marketing authorisation holder | Dr. Franz Köhler Chemie GmbH |
| Distributor | Grünenthal Österreich GmbH |
| Batch number(s) | 1. Batch, Expiry Date 2324111, 31.07.2025 2213911, 30.04.2024 2. Batch, Expiry Date 2308911, 28.02.2025 2217911, 31.05.2024 2314311, 30.04.2025 2202711, 31.12.2023 |
| Classification of the recall | 2 |
| Depth of recall | Pharmacies |
| BASG reference number | INS-640.001-4780 |
Further inquiry note
Page last modified:
12/07/2024