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 ...

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 ...

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 ...

Washington (CNN)-- Millions of needles used in ports implanted under the skin of chronically ill patients are being voluntarily recalled, the U.S. Food and Drug Administration announced Tuesday. More ...

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 ...

Huber needles are specialized medical devices designed for accessing implanted ports or catheters, commonly used in long-term medical treatments such as chemotherapy or parenteral nutrition. These ...

DUBLIN--(BUSINESS WIRE)--Research and Markets has announced the addition of the "European Market Report for Port Needles 2017 - MedCore" report to their offering. Over the forecast period, the total ...

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 ...