Guidant Recall
On June 17, 2005, Guidant issued a voluntary recall of its implanted cardiac defibrillator. The Guidant recall is linked to at least 45 failures of the device and the deaths of two patients.
Guidant Defibrulator Lawsuit

Guidant Recall Information
About Defibrillators
About Pacemakers
Contact an Attorney
FDA Recalls Guidant Pacemaker
Guidant Pacemaker Recall
Guidant Press Release
Health Related Links
Recalled Defribrillators
Recent FDA Updates Concerning Guidant

Claim Information
Heart Conditions and Diseases
Heart Health

 

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File a Claim for the Guidant Defibrulator Recall

The following models, all manufactured between November 25, 1997 and October 26, 2000, have been included in the recall:  

GUIDANT PULSAR MAX Models

·         Pulsar Max 1170

·         Pulsar Max 1171

·         Pulsar Max 1270

GUIDANT PULSAR Models

·         Pulsar 0470

·         Pulsar 0870

·         Pulsar 0970

·         Pulsar 0972

·         Pulsar 1172

·         Pulsar 1272

GUIDANT DISCOVERY Models

·         Discovery 1174

·         Discovery 1175

·         Discovery 1273

·         Discovery 1274

·         Discovery 1275

GUIDANT MERIDIAN Models

·         Meridian 0476

·         Meridian 0976

·         Meridian 1176

·         Meridian 1276

GUIDANT PULSAR MAX Models

·         Pulsar Max II 1180

·         Pulsar Max II 1181

·         Pulsar Max II 1280

GUIDANT DISCOVERY II Models

·         Discovery II 0481

·         Discovery II 0981

·         Discovery II 1184

·         Discovery II 1186

·         Discovery II 1187

·         Discovery II 1283

·         Discovery II 1284

·         Discovery II 1285

·         Discovery II 1286

GUIDANT CONTAK TR Model

·         Contak TR 1241

GUIDANT VIRTUS PLUS II

·         Virtus Plus II 1380

·         Virtus Plus II 1480

GUIDANT INTELIS II Models

·         Intelis II 1483

·         Intelis II 1484

·         Intelis II 1485

·         Intelis II 1384

·         Intelis II 1385

·         Intelis II 1349

·         Intelis II 1499

If you have been injured as a result of any of the above Guidant Pacemakers, you may be entitled to monetary compensation.  For a free review of your claim, please fill out the form below.  A lawyer will review your form and may contact you to discuss your case.

Free Recalled Defribrillators Consultation

Title:
First Name: *
Middle Name:
Last Name: *
Home Phone: *
Cell Phone:
Work Phone:
Email Address:
Address: *
City: *
State, Zip: *    *

What is the best way to reach you?
Please provide the best place, time and
method for contacting you.

               Date of Implantation:   *

Type of Guidant Cardiac Device implanted:
(name, model no., serial no.)
*

What hospital implanted the device?
Name of Hospital: *
Address: *
City: *
State: *
Zip Code: *
Phone: *

Please attach a copy of papers of Identification card identifying your
Guidant Cardiac device when you return your completed packet to us.
Do you have a copy of the identification card 
identifying your Guidant Cardiac device? 		Yes    No
What is the date you 
experienced your injury? 		  *
Have you had an explant? Yes    No
What was the date of the explant?   

Case Description*
Please explain exactly what happened, trying to state
as thoroughly as possible who you believe was responsible
and why you believe that person was negligent:
Comments / Additional Information
Is there anything else that would assist us in
understanding the facts of your case?

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please tell us which search engine?
Please tell us exactly what terms you typed into the
search engine to find us? (i.e. Personal Injury Lawyers)
I understand that by filling out this free consultation form I am not forming an attorney client relationship. I understand that I may only retain an attorney by entering into a fee agreement and that by submitting this form I am not entering into a fee agreement. I understand that not all submissions may receive a response.
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I agree that the above does not constitute a request for legal advice. I agree that any information that I will receive in response to the above question is general information and I will not be charged for the response to this e-mail question. I further understand that the law for each state may vary, and therefore, I will not rely upon this information as legal advice. I agree that if this matter requires advice regarding my home state, local counsel may be contacted for referral of this matter. I understand that email is not secure and thus I am not forming a confidential relationship.
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Click on Your Model to Contact an Attorney

Guidant Recall Defibrillators

 

Guidant Pacemakers Recalled

 

Guidant CRT and Defibrillator Model Numbers:

 

Guidant Pacemaker Model Numbers Recalled:

  • 0470
  • 0476
  • 0481
  • 0870
  • 0970
  • 0972
  • 0976
  • 0981
  • 1170
  • 1171
  • 1172
  • 1174
  • 1175
  • 1176
  • 1180
  • 1181
  • 1184
  • 1186
  • 1187
  • 1241
  • 1270
  • 1272
  • 1273
  • 1274
  • 1275
  • 1276
  • 1280
  • 1283
  • 1284
  • 1285
  • 1286
  • 1349
  • 1380
  • 1384
  • 1385
  • 1480
  • 1483
  • 1484
  • 1485
  • 1499

CRT

  • Contak Renewal
  • Contak Renewal 2
  • Contak Renewal 3 (Class II)
  • Contak Renewal 4 (Class II)
  • Contak Renewal Model H135 (Class I)
  • Contak Renewal Model H155 (Class I)
  • Renewal AVT (Class II)
  • Renewal 3 AVT (Class II)
  • Renewal 4 AVT (Class II)
  • Renewal RF (Class II)

 

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For Case Related Inquiries Contact:
Justin R. Cook, Esquire
(888)423-4477
(617) 227-7000

_____________________________

Sheff Law Offices, P.C.
10 Tremont Street
Boston, MA 02108
(888) 423-4477

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