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 ...
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 ...
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 ...
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