Class 3 Medicines Recall: Glenmark Pharmaceuticals Europe Ltd, Fingolimod 0.5 Mg Hard Capsules, El(24)a/39
Recall Summary Glenmark Pharmaceuticals Europe Ltd is recalling Fingolimod 0.5 mg hard capsules (batch details specified in the recall notice) distributed in the United Kingdom because retesting found the product did not meet required specifications. This recall affects anyone in the UK who may have this medication.
- Product
- Glenmark Pharmaceuticals Europe Ltd is recalling this batch after retesting showed out of specification results.
- Reason
- Glenmark Pharmaceuticals Europe Ltd is recalling this batch after retesting showed out of specification results.
- Classification
- Class II
- Category
- drug recall
- Country
- United Kingdom
- Agency
- UK Medicines and Healthcare products Regulatory Agency
- Recall date
- 2024-08-19
- Status
- Ongoing
- Distribution
- United Kingdom
Official recall notice from UK Medicines and Healthcare products Regulatory Agency
Recall details on Nibble Recalls: https://trynibble.app/recalls/9e76ce9b-137c-4488-82cc-168133b37f65