http://www.medpagetoday.com/PublicHealthPolicy/FDAGeneral/36621?utm_content=&utm_medium=email&utm_campaign=DailyHeadlines&utm_source=WC&xid=NL_DHE_2012-12-27&eun=g578717d0r&userid=578717& From the article… The FDA has issued a class I recall of two infusion pumps citing motor failure when used with drugs not specifically approved for them. Device manufacturer Medtronic noted in a letter sent to healthcare professionals that the device failure rate went from 2.4% when used with approved drugs to 7% […]
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