FDA Recalls Finder

FDA Announces Class I Recall of Certain Infusion Set Needles
26 January 2010, 9:47 am

The U.S. Food and Drug Administration today announced a Class I recall of Exel/Exelint Huber needles, Exel/Exelint Huber Infusion Sets and Exel/Exelint “Securetouch+” Safety Huber Infusion Sets, manufactured by Nipro Medical Corporation for Exelint International Corporation.

Source: Food and Drug Administration--Press Releases