Class 2 Medicines Recall: Flutiform 250 Micrograms / 10 Micrograms Per Actuation Pressurised Inhalation, Suspension , Cd Pharma Ltd, El(25)a/35
Recall Summary Flutiform 250/10 micrograms inhalation suspension made by CD Pharma Ltd has a labeling error on certain batches where the delivered dose information on the outer carton is incorrect, though the total active content is accurate and all other carton details are correct. This recall affects products distributed in the United Kingdom. The MHRA classified this as a Class II recall due to the mislabeling on the packaging.
- Recalling firm
- Flutiform 250 micrograms / 10 micrograms per actuation pressurised inhalation
- Reason
- CD Pharma Ltd have notified the MHRA of an error on the outer carton of the product for the batches listed in this notification. While the total active content statement is correct, the delivered dose content statement is incorrect. The other details on the carton are correct.
- Classification
- Class II
- Category
- drug recall
- Country
- United Kingdom
- Agency
- UK Medicines and Healthcare products Regulatory Agency
- Recall date
- 2025-07-24
- 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/1b08d186-edcb-4d62-9b76-ff34a4edb2dd