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Insulin pen recall - NovoPen 5 and Echo Posted on 25 Aug 2017

on 24th August 2017, the MHRA (Medicines & Healthcare Products Regulatory Agency) issued a Medical Device Alert, following a Field Safety Notice issued in July by Novo Nordisk - the manufacturer of NovoPen 5 and NovoPen Echo.

The practice has written to all patients who have been prescribed these products since July 2014 as a precaution, although the likelihood of having an affected device is minimal.

A copy of the notice from Novo Nordisk is available here to download.

Field safety Notice - NovoPen 5 and Echo

All queries should be directed to Novo Nordisk customer services on 0845 600 5055, not to the surgery. 

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