Lenalidomid Mylan Hartkapseln
Recall
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Medicines
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03/10/2025
The marketing authorisation holder informed its customers on October 03,2025, that due to the possible presence of powder in the blister pouches, the mentioned batches of the medicinal product are being recalled as a precautionary measure.
| Name of the medicinal product | 1. Lenalidomid Mylan 2,5 mg Hartkapseln 2. Lenalidomid Mylan 5 mg Hartkapseln 3. Lenalidomid Mylan 7,5 mg Hartkapseln 4. Lenalidomid Mylan 10 mg Hartkapseln 5. Lenalidomid Mylan 15 mg Hartkapseln |
|---|---|
| Marketing authorisation number(s) | 1. 0-93912 2. 0-93913 3. 0-93914 4. 0-93915 5. 0-93916 |
| CIP code | 1. 5504219 2. 5504225 3. 5504231 4. 5504248 5. 5504254 |
| Marketing authorisation holder | Mylan Pharmaceuticals Limited |
| Distributor | Viatris Austria GmbH |
| Batch number(s) | 1. Batch, Expiry Date 8165889, 07/2026 2. Batch, Expiry Date 3179807, 04/2026 3. Batch, Expiry Date 8171013, 06/2026 8179823, 02/2027 4. Batch, Expiry Date 8155319, 01/2026 8174610, 10/2026 5. Batch, Expiry Date 8201459, 01/2028 |
| Classification of the recall | 2 |
| Depth of recall | Pharmacies |
| BASG reference number | INS-640.001-5185 |
Further inquiry note
Page last modified:
02/10/2025