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, ...

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 ...

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 Administration ...

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 ...

Huber needles used in implanted ports to withdraw blood, inject medications, and other solutions SILVER SPRING, Md., Jan. 26 /PRNewswire-USNewswire/ -- The U.S. Food and Drug Administration today ...

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 ...