How do I know if I have a recalled Medtronic heart device?

This situation is limited to a group of implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillator (CRT-Ds) incorporating batteries manufactured between April 2001 and December 2003 that were implanted in patients.
Specifically, devices include:

• Model 7230 Marquis VR
• Model 7274 Marquis DR
• Model 7232 Maximo VR
• Model 7278 Maximo DR
• Model 7277 InSync Marquis
• Model 7289 InSync II Marquis
• Model 7279 InSync III Marquis
• Model 7285 InSync III Protect (no devices implanted in the United States)

To clarify whether your device is in this group, please call your physician or the Medtronic patient toll-free line at 1-800-551-5544 (M-F, 7 a.m. - 6 p.m. CT) .

The information on this page is meant to provide a general overview of the law. The laws in your state and/or city may deviate significantly from those described here. If you have specific questions related to your situation you should speak with a local attorney.

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