Becker's Hospital Review

FDA Recalls Certain Huber Infusion Needles

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, ...
Medscape

FDA Issues 2 Recalls of Huber Needles

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 ...
Medscape

FDA Expands Recall of Huber Needles

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 ...
Mena FN

Global Huber Needles Market Analysis By Size & Share: Cagr Of 6.15% Expected To Achieve Usd 78 Million By 2030

Port access systems allow for the administration of drugs and fluids as well as the collection of blood samples without the need for many needle jabs to be performed. These ports are implanted ...
Daily Herald

FDA announces recall of 2 million defective needles

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 ...
Richmond

FDA recalls 2 million defective needles

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

FDA recalls 2M defective needles

WASHINGTON, D.C. -- 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 ...