FDA Announces Class I Recall of Certain Infusion Set Needles

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Title: FDA Announces Class I Recall of Certain Infusion Set Needles

FDA Announces Class I Recall of Certain Infusion Set Needles
Tue, 26 Jan 2010 09:47:00 -0600

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.


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