Resource Library

Free Online Legal Resources

What defibrillator models are being recalled?

The Guidant defibrillators affected by this recall are:

• PRIZM 2 DR, Model 1861, manufactured on or before April 16, 2002
• CONTAK RENEWAL, Model H135, manufactured on or before August 26, 2004
• CONTAK RENEWAL 2, Model H155, manufactured on or before August 26, 2004

Guidant also recently informed the FDA that they are recalling another set of defibrillator devices called PRIZM AVT, VITALITY AVT, RENEWAL 3 AVT and RENEWAL 4 AVT. The company reports the devices are subject to a memory error, which may affect therapy and device performance.

Speak to an Experienced Guidant Attorney Today

This article is intended to be helpful and informative. But even common legal matters can become complex and stressful. A qualified guidant lawyer can address your particular legal needs, explain the law, and represent you in court. Take the first step now and contact a local guidant attorney to discuss your specific legal situation.

Your Next Step:

Enter your location below to get connected with a qualified Guidant attorney today.

Additional Guidant Articles

Search LawInfo's Guidant Resources

Guidant Videos

What is Your Case Worth

Guidant Lawyers