The U.S. Food and Drug Administration has issued a Class I recall of Exel/Exelint Huber needles, Exel/Exelint Huber Infusion Sets and Exel/Exelint “Securetouch+” Safety Huber Infusion Sets, ...
August 27, 2010 — The US Food and Drug Administration (FDA) has issued 2 class 1 recalls of Huber needles due to cases of coring when inserted into ports. "Coring may lead to infection, damage or ...
October 13, 2010 — An earlier class 1 recall of Huber needles by the US Food and Drug Administration (FDA) on account of coring — which is potentially life-threatening — has been broadened to include ...
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