Previous Investigations
Other Litigations Guidant Defibrillator Research Center News & Warnings
|
Guidant Recalls Dangerous Defibrillator Models
|
BREAKING NEWS: 10.15.07--Medtronic, Inc., the world's largest maker of electronic heart devices, announced they are suspending sales of Sprint Fidelis leads. According to the FDA, these wires, used to connect defibrillators to the heart, may break or erode and may increase chance of injury. Learn more about the Medtronic Sprint Fidelis Recall. |
The following is a list of defibrillator models have been recalled by the Guidant Corporation after it admitted serious design flaws, which may be harmful to your health and may ultimatly lead to death.
| Device | Model(s) | Manufactured Before | Failures | Deaths |
|---|---|---|---|---|
| VENTAK PRIZM 2 dr | 1861 | Apr-02 | 28 | 1 |
| CONTAK RENEWAL | H135, H155 | 6-Aug-04 | 15 | 1 |
| VENTAK PRIZM AVT | NA | NA | 2 | 0 |
| VITALITY AVT | NA | NA | 2 | 0 |
| RENEWAL 3 AVT | NA | NA | 2 | 0 |
| RENEWAL 4 AVT | NA | NA | 2 | 0 |
If you or a loved one has been injured by one of these models, do not wait to get help, fill out a form today to have your case evaluated for FREE. An experienced attorney can help get you compensation for your medical bills, mental anguish and other related expenses.
Weitz & Luxenberg is no longer accepting Guidant Defibrillator cases.
see also:
Weitz & Luxenberg Release
Our Press Release About Guidant Defibrillator RecallRecall of Guidant Defibrillators - Do You Have a Case?
Guidant Warning
Recalled Guidant Defibrillator *WARNING* from AttorneysGuidant *WARNING* - Recalled Models: Learn how an attorney can help
Recall
Guidant Defibrillator: Learn the dangers and how a lawsuit can helpLearn more about the Guidant Defibrillator lawsuit
