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 ...
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 ...
NEW YORK, April 30, 2018 /PRNewswire/ -- Persistence Market Research provides key insights and forecast on the global Huber needles market for the forecast period 2017-2024.The primary objective of ...
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 ...
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