The US Food and Drug
Administration in cooperation with
Sanofi has announced the recall
of all lots of the company’s Auvi-Q
epinephrine injection product
line, because the devices may not
deliver the correct dose.
The US recall includes all 0.15mg
and 0.3mg autoinjectors with lot
numbers 2299596-303720 and
labelled expiration dates of Mar-
Dec 2016.
Sanofi said it had received 26
reports of suspected “device
malfunctions,” and has advised
patients to contact their healthcare
provider to obtain a prescription for
an alternate autoinjector.The above article was sent to subscribers in Pharmacy Daily's issue from 03 Nov 15 To see the full newsletter, see the embedded issue below or CLICK HERE to download Pharmacy Daily from 03 Nov 15
THE role and significance of community pharmacy in regional areas was a key focus of discussion for the Nationals leader David Littleproud during last week’s visit to Orana Mall Pharmacy as part of a regional tour.
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