Recall Notice for Ketofall 0.25 mg/ml Eye Drops Solution – PA1815/002/001

We would like to bring to your attention an important recall notice regarding Ketofall 0.25 mg/ml Eye Drops Solution in single-dose containers.


Background Information:

The Health Products Regulatory Authority (HPRA) has issued a recall notice for Ketofall 0.25 mg/ml Eye Drops Solution in single-dose containers, with the authorization number PA1815/002/001. This recall has been initiated due to concerns related to product quality and safety.


Potential Risks:

While there have been no reported adverse effects associated with the affected product, it is crucial to follow the guidance provided in the official recall notice. The recall is being undertaken as a precautionary measure to prevent any potential risks to patients.


Next Steps for Patients:

If you have been prescribed Ketofall 0.25 mg/ml Eye Drops Solution, please consult with your healthcare provider immediately. They will be able to provide you with further guidance regarding alternative treatment options or discuss any necessary adjustments to your current treatment plan.


Next Steps for Healthcare Professionals:

Healthcare professionals are advised to stop dispensing and using the affected product. Please refer to the official recall notice for detailed instructions on returning the recalled medicine and obtaining replacement stock.


Contact Information:

For any questions or concerns related to this recall, please contact the relevant authority as provided in the official recall notice linked here :



Ensuring patient safety and providing accurate information is our top priority. We encourage all patients and healthcare professionals to stay informed about recalls and take appropriate action when necessary.


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