SHANGHAI, SHANGHAI, CHINA, June 11, 2026 /EINPresswire.com/ — As long-term vascular access therapies continue to expand across oncology, infusion treatment, and ...
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 ...