January 26, 2010 — A class I recall of 2 million Huber needles manufactured by Nipro Medical Corporation and distributed by Exelint International Corporation was announced today by the US Food and ...

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, ...

WASHINGTONWASHINGTON — Federal health officials announced the recall of 2 million medical needles Tuesday because of a risk they can push bits of silicone into patients’ bodies. The Food and Drug ...

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 ...

Federal health officials announced the recall of 2 million medical needles Tuesday because of a risk they can push bits of silicone into patients' bodies. The Food and Drug Administration said ...

WASHINGTON -- Federal health officials announced the recall of 2 million medical needles Tuesday because of a risk they can push bits of silicone into patients' bodies. The Food and Drug ...

Huber needles are not created with a coring tip like conventional needles are, hence they are distinguished from regular needles by this distinction. During the insertion and withdrawal processes, a ...

The article purports to present the most important studies on complications in port catheter systems from the past 10 years. This may be the reason for the error when ...

Federal health officials announced the recall of 2 million medical needles Tuesday because of a risk they can push bits of silicone into patients' bodies. The Food and Drug Administration said ...

U.S. federal health officials announced the recall of two million medical needles Tuesday because of a risk they can push bits of silicone into patients' bodies. The U.S. Food and Drug Administration ...