Emerade is subject to Class 1 Product Recall by the manufacturer Pharmaswiss Česka republika s.r.o. For more details please follow the link below:

https://www.gov.uk/drug-device-alerts/national-patient-safety-alert-class-1-medicines-recall-notification-recall-of-emerade-500-micrograms-and-emerade-300-micrograms-auto-injectors-due-to-the-potential-for-device-failure-natpsa-slash-2023-slash-004-slash-mhra