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.
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.