Class 2 Recall on Emerade Auto-Injectors Bausch & Lomb UK

Recalls and Alerts

Class 2 Recall

Class 2 Recall on Emerade Auto-Injectors Bausch & Lomb UK

Pharmaswiss Česka republika s.r.o. (an affiliate of Bausch & Lomb UK Limited) is recalling all unexpired batches of the above product due to an error in one component of the autoinjector believed to cause some pens to fail to activate and deliver adrenaline.

Please visit the: MHRA website for more details on this drug alert.

The affected products' details are as follows:

PIP Code	Product Description	Supplier	Affected Batch
3849221	EMERADE 150 AUTO-INJECTOR	BAUSCH & LOMB UK	ALL STOCK
3849239	EMERADE 300 AUTO-INJECTOR	BAUSCH & LOMB UK	ALL STOCK
3849247	EMERADE 500 AUTO-INJECTOR	BAUSCH & LOMB UK	ALL STOCK

Please note that Alliance Healthcare do not stock and as this is a caution in use only we are not accepting stock returns.

For stock enquiries please contact Bausch & Lomb Customer Services: Tel: 0208 781 2991 Email: Pharma_CS@bausch.com.

For medical information enquiries please contact the Pharmacovigilance and Medical Information Officer, Tel: 0208 781 5523, Email: Pharmacovigilance.UK@bausch.com

Recipients of this Drug Alert should bring it to the attention of relevant contacts.

Please return all affected stock to your original supplier for credit.

If you have any questions, then please contact your local Service Centre Customer Services team.