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DEFECTIVE MEDICAL DEVICES

Parker Waichman Alonso LLP is a leader in a defective medical device litigation. We are currently evaluating cases involving the medical devices listed below. Please click on a specific medical device or fill out the form at the right for a free case evaluation by a qualified attorney.

Defective Medical Devices

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Medtronic Cardiac Rhythm Disease Management Site Gets FDA Warning Letter

Nov 19, 2009 | Parker Waichman Alonso LLP
Device maker giant, Medtronic, Inc., just announced that it received a warning letter from the U.S. Food & Drug Administration (FDA).According to...

CSI Says ViperSheath Sheath Introducer Could Break, Recall Issued

Nov 18, 2009 | Parker Waichman Alonso LLP
Cardiovascular Systems Inc (CSI) has initiated a recall of all lots of the ViperSheath Sheath Introducer on behalf of Thomas Medical.  According...

Negative Pressure Wound Therapy Warning From FDA Following Death, Injury Reports

Nov 17, 2009 | Parker Waichman Alonso LLP
The use of Negative Pressure Wound Therapy systems have been associated with deaths and serious complications, the U.S. Food & Drug...

Zinc in Fixodent, Super PoliGrip Linked to Nerve Damage By Another Study

Nov 16, 2009 | Parker Waichman Alonso LLP
Super PoliGrip,  Fixodent and other denture creams have been associated with nerve damage and the  development of neurological problems,...

Synthes USA Issues Class I Recall for Vertebrae Replacement Implants

Nov 13, 2009 | Parker Waichman Alonso LLP
Synthes USA is recalling all lots of the Ti Synex II Vertebral Body Replacement device.   The U.S. Food & Drug Administration (FDA) has...

FDA Investigating Problems With External Biphasic Defibrillators

Nov 11, 2009 | Parker Waichman Alonso LLP
The U.S. Food and Drug Administration (FDA) is investigating energy levels in external biphasic defibrillators with shocks ≤ 200 J. The agency...

Edwards Lifesciences Recalls Aortic Catheters

Nov 10, 2009 | Parker Waichman Alonso LLP
Edwards Lifesciences Corporation has issued a recall of CardioVations EndoClamp Aortic Catheter.  The Food & Drug Administration (FDA) has...

Centurion Premie and Meconium Packs Recalled

Nov 5, 2009 | Parker Waichman Alonso LLP
Centurion Medical Products Premie Pack and Meconium Pack Pediatric Tracheal Tubes have been recalled, the U.S. Food and Drug Administration (FDA)...

More Claims Filed over Medtronic Sprint Fidelis Leads

Nov 5, 2009 | Parker Waichman Alonso LLP
Three more lawsuits have been filed against Medtronic, Medtronic USA, Medtronic International Technology, and Medtronic Puerto Rico Operations,...

Cordis Recalls Crossover Sheath Introducer

Nov 2, 2009 | Parker Waichman Alonso LLP
Cordis Corporation is recalling all lots of the Crossover Sheath Introducer due to complaints about stretching or fracture of the sheath during use....

Stryker Biotech, Execs Indicted for Alleged Illegal Promotion of Bone Growth Product

Oct 30, 2009 | Parker Waichman Alonso LLP
Stryker Biotech LLC has been indicted on federal charges of illegally marketing bone growth products called the OP-1 Implant and OP-1...

Qualitest Pharmaceuticals Issues Recall For All Accusure® Insulin Syringes

Oct 28, 2009 | Parker Waichman Alonso LLP
A voluntary nationwide recall was issued yesterday for all Accusure® Insulin Syringes manufactured by Qualitest Pharmaceuticals of Huntsville,...
Defective Medical Devices
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