FDA Classifies Labeling Corrections Related to Occurrence of Pocket Fills During a SynchroMed® Implantable Infusion Pump Refill as a Class I Recall

FDA Classifies Labeling Corrections Related to Occurrence of Pocket Fills During a SynchroMed® Implantable Infusion Pump Refill as a Class I Recall

Submitted by moderatora on February 16, 2011 - 11:53am
Source: 
Yahoo/Businesswire
News Tags: 
FDA
recalls
Medtronic
Pocket Fills
SynchroMed II
SynchroMed EL
infusion pumps
Headline: 
FDA Classifies Labeling Corrections Related to Occurrence of Pocket Fills During a SynchroMed® Implantable Infusion Pump Refill as a Class I Recall

Do Not Allow Advertisers to Use My Personal information