Medscape

FDA Device Clearances: Neurostimulation Lead, Power Injectable Ports and Safety Needles, Automated Blood Testing Instrument

June 26, 2007 — The US Food and Drug Administration (FDA) has granted premarket approval for a neurostimulation lead for chronic pain management, and 510(k) clearance for power injectable ports and ...
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 ...
NBC News

2 million faulty needles recalled by FDA

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 ...
Medscape

2 Million Huber Needles Recalled Because of Coring Defect

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 ...