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Urgent recall of asthma inhaler issued by MHRA
A labelling error on the Flutiform inhaler leads to an urgent recall in the UK.
Health authorities in the UK have recalled a popular asthma inhaler over a labelling mistake.
Urgent recall of asthma inhaler due to labelling error
The Medicines and Healthcare products Regulatory Agency (MHRA) has issued a recall of the Flutiform 250 micrograms inhaler after CD Pharma Limited reported a labelling error on specific batches. The active ingredient content on the packaging is correct, but the dosage information is misleading, suggesting patients may receive less medication than intended. The inhaler is safe and effective, and patients are advised not to stop using it as prescribed. The recall affects pharmacies and wholesalers across the UK, emphasizing that the inhaler's safety is not in question.
Key Takeaways
"This is a wholesale and pharmacy level recall that will be actioned by a healthcare professional."
The MHRA confirms the recall process will involve healthcare professionals.
"There is no quality issue with the product and patients can continue to take their medicine as prescribed."
The MHRA reassures patients about the inhaler’s effectiveness despite the recall.
This incident highlights the critical need for accuracy in pharmaceutical labeling, especially for medications managing chronic conditions like asthma. With the potential for anxiety among patients misinformed about their dosage, immediate action from health authorities is vital. The MHRA's prompt response underscores its commitment to patient safety, ensuring that while the product continues to be used safely, proper communication is vital to prevent panic and confusion among users.
Highlights
- Misleading labels can lead to unnecessary anxiety for patients.
- Accurate medication information is essential for patient safety.
- Pharmacy recalls are vital in maintaining public trust in healthcare.
- Patients should feel reassured that their inhaler is still safe.
Concerns over patient safety and potential confusion
The incorrect dosage information could create unnecessary anxiety for patients managing asthma. Immediate clarification is needed to prevent public panic.
This incident calls for heightened vigilance in pharmaceutical standards and communication.
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