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GUIDANT CORP. CLASS ACTION.

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GUIDANT CORP. PACEMAKER* RECALL (implantable cardioverter-defibrillators): Guidant Corporation Information

As you may know from viewing our main "Guidant Recall" page, Guidant has recalled the following ICDs (implantable cardioverter-defibrillators):

  • VENTAK PRIZM 2 DR (Model 1861) ICDs manufactured on or before April 16, 2002.
  • CONTAK RENEWAL (Model H135) and CONTAK RENEWAL 2 (Model H155) CRT-Ds manufactured on or before August 26, 2004.
  • VENTAK PRIZM AVT, VITALITY AVT, RENEWAL 3 AVT and RENEWAL 4 AVT ICDs (All series numbers).

If you have been implanted with any of these devices, you are urged to contact our law firm immediately to protect your legal rights.

Below is some additional information regarding Guidant, the manufacturer of the ICDs that have been recalled (all links will open in new window):

"Uncertainty has engulfed the announced $25 billion purchase by Johnson & Johnson of Indianapolis' Guidant Corp., facing a huge defibrillator recall."
-
Guidant deal with J&J may be in danger:

"Last week, Guidant recalled 50,000 implantable defibrillators that could malfunction in a small number of cases after it was revealed that the company failed to notify doctors for three years about a possible flaw in one model."
- FDA: Medtronic didn't fix defibrillator flaws

"Guidant Corp. (GDT.N: Quote, Profile, Research) on Friday said it was recalling 50,000 of the devices after two deaths and several reports of device failure. The company in May had warned doctors that some of the products contained a flaw, but it did not recommend that they be replaced because the risks of doing so outweighed any dangers the device might pose."
- Group to set defibrillator recall standards

"On Monday, Guidant shares were down $1.51, or 2%, to $70.95. The company said Friday that 50,000 of its implantable cardiac defibrillators in service could be subject to defects that have led to 45 malfunctions. The company has warned doctors worldwide about possible problems with some of the devices. Two patients with defibrillators covered by the notification have died."
- Device Trouble Trips Guidant

"Several Thousand defibrillators will be recalled after the U.S. Food and Drug Administration (FDA) ordered manufacturer Guidant Corp, to retire three of its models from the marketplace. Reports of 45 "failures" and two deaths caused the FDA to ponder its policy."
- Defibrillators recalled as failures multiply

[emphasis added in all quotes]

Our law firm is currently investigating potential personal injury and/or class action cases against Guidant, and if you think that you may have been harmed by your Guidant ICD (pacemaker), you are strongly encouraged to contact us. There is no charge, and no obligation. If we take your case, there is no fee for our services unless we win your case, or settle it in your favor.

If you have been implanted with any of these devices, you are urged to contact our law firm immediately to protect your legal rights.

On the other hand, if you fail to protect your legal rights now, you may lose the right to be compensated for your harm. (Persons seeking to preserve any potential legal claims should contact an attorney promptly, since all states have mandatory time periods in which lawsuits must be filed with the courts; otherwise, they may be forever barred).

Our firm has a great deal of experience in representing plaintiffs in “defective medical device ” cases, and in fact, is currently pursuing cases against Guidant for their "Ancure" stent device.

In addition, we have the resources to handle our own cases. This means that when you call our firm, you talk to your own lawyer who has been assigned to your own case.

Please contact us now (your privacy is assured). The secure form below only takes a couple of minutes to fill out, but if you are uncomfortable sending your information over the internet, please call our toll-free number at 800.921.1776 to speak to an attorney. The call is free, and there is no obligation. Act now, as delays can harm your case.

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Persons seeking to preserve any potential legal claims should contact an attorney promptly, since all states have mandatory time periods in which lawsuits must be filed with the courts; otherwise, they may be forever barred.

About Our Firm: [^]

Alexander Hawes, LLP, an AV-rated trial firm, has concentrated its practice on the prosecution of complex Personal Injury and Class Action cases. The Firm represents individuals, governmental entities, businesses and institutional shareholders in auto accident cases, insurance claims, motorcycle injury accidents, and truck (and SUV) accidents. In addition, our law firm represents consumers in defective product, product liability, tort, negligence, mass tort, consumer, construction defect, investment fraud, price fixing and employment cases. The Firm is currently involved in complex cases pending in federal and state courts throughout the Unites States. The Firm is dedicated to quality representation of its clients and prides itself on aggressive advocacy of its clients' claims.

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