April 26, 2005 — The U.S. Food and Drug Administration (FDA) and Medtronic, Inc., have notified customers via letter of the expansion of a class 1 recall of 1.924 monophasic LIFEPAK 500 automated ...
SAN FRANCISCO (MarketWatch) -- Medtronic Inc. said after the bell Friday that it is recalling 1,924 Lifepak 500 automatic external defibrillators that were made in 1997 because some of the devices ...
March 2, 2005 — The U.S. Food and Drug Administration (FDA) and Medtronic, Inc., have notified customers via letter of a class 1 recall of a limited number of monophasic LIFEPAK 500 automated external ...
REDMOND, WASH. – Feb. 19, 2010 – Physio-Control Inc., a wholly-owned subsidiary of Medtronic, Inc. (NYSE: MDT), announced today it received notice from the U.S. Food and Drug Administration (FDA) that ...
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