News » MHRA alert » Alert: Flutiform 250 micrograms / 10 micrograms per actuation
July 25th 2025
CD Pharma Ltd is recalling four batches of Flutiform 250 micrograms / 10 micrograms per actuation pressurised inhalation, suspension (fluticasone propionate/formoterol fumarate) due to a packaging error.
The affected batches are:
| Batch No. | Expiry Date | Pack Size | First Distributed |
|---|---|---|---|
| 270185-24062FA-30424 | 30 Jun 2026 | 120 Actuations | 30 Jun 2025 |
| 270186-24065FA-30443 | 30 Jun 2026 | 120 Actuations | 04 Jul 2025 |
| 270774-24082FB-30444 | 31 Jul 2026 | 120 Actuations | 04 Jul 2025 |
| 269881-24064FA-30425 | 30 Jun 2026 | 120 Actuations | 04 Jul 2025 |
The error relates to the outer carton of the product which contains an incorrect delivered dose content statement. The other product details on the carton, including the name, strength and pharmaceutical form of the medicine are correct. The quality of the medicine is not impacted by the labelling defect.
Healthcare professionals are asked to quarantine all stock and return it to your supplier using your supplier’s approved process. Patients should continue to take the medication as prescribed.
For all further enquiries please contact 01355 204 448 or email regaffairs@teleta.co.uk
