Guidant is voluntarily advising physicians about important safety information regarding certain pacemaker devices. The company alerted the FDA, which could lead to recalls. Among the devices in question are PULSAR MAX, PULSAR, DISCOVERY, MERIDIAN, PULSAR MAX II, DISCOVERY II, VIRTUS PLUS II, INTELIS II, and CONTAK TR, any of which that were manufactured between November 25, 1997 and October 26, 2000.
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