Class 4 Medicines Defect Notification: Sirdupla 25 Microgram/250 Microgram Per Metered Dose Pressurised Inhalation, Suspension, El(25)a/12
Sirdupla Inhaler Recall Summary Sirdupla 25 microgram/250 microgram inhalers from batch 77518 are being recalled in the United Kingdom due to a printing defect on the outer label. The defect affects the labeling on the product packaging. This recall applies to all users of this specific batch of the medication.
- Recalling firm
- Sirdupla 25 microgram/250 microgram per metered dose pressurised inhalation
- Reason
- Cross Healthcare Limited have informed the MHRA that there is a printing defect on the outer labels for the Sirdupla 25 microgram/250 microgram per metered dose pressurised inhalation, suspension, batch 77518.
- Classification
- Class III
- Category
- drug recall
- Country
- United Kingdom
- Agency
- UK Medicines and Healthcare products Regulatory Agency
- Recall date
- 2025-03-31
- 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/2d7cdbdf-4600-4c6e-a6bf-66dd92196683