Drugs and Devices

Hospira infusers recalled

On Sept. 10, the U.S. Food and Drug Administration announced the recall of the Hospira Symbiq One-Channel and Two-Channel Infusers because of the potential of the device to fail to detect air in the line at the end of an infusion. Read more here.


Related Articles:

Leave a Reply

Your email address will not be published. Required fields are marked *

 

Shares