We are no longer accepting cases for this medical device.

MEMPHIS, TN — Attorneys Tim Edwards and Ed Wallis are announcing that the deaths of five users of a small mechanical heart pump have prompted the manufacturer to recall the device. According to device maker Thoratec Corp., wear on an electrical wire in the implant may cause the devices to fail. The recall applies to heart pumps distributed to 153 hospitals and other locations since 2003.

The recall affects devices with catalog numbers 1355 and 102139.

Reports have shown an alarming failure rate: 1.3% at 12 months, 6.5% at 24 months and 11.4% at 36 months.

The FDA has urged patients with the Heartmate II to contact their doctors to have the device checked. Surgery to have the faulty medical device replaced will be an option for some however for those who are not good candidates for re-surgery the device will be allowed to fail resulting in the death of the patient.

Mr. Edwards and Mr. Wallis represent injured persons who have been implanted with dangerous and defective medical devices. They are prepared to offer a free case evaluation to you today. If you have a recalled device, please see your medical provider immediately. If you or a loved one have sustained injuries from a recalled Heartmate II device, or wish to discuss your rights for a lawsuit against Thoratec Corp., please contact us today by calling Tim Edwards and Ed Wallis at (901) 527-2125, or via e-mail by clicking HERE.

Mr. Edwards and Mr. Wallis are currently representing injured children and adults on an international level for a failed medical device.  Both have represented clients, filed lawsuits and appeared in courts around the country to protect the rights of the injured including for the Advanced Bionics HiRes90k cochlear implant, the transvaginal mesh device, the Heartmate II, Composix® Kugel® Mesh Hernia Repair Patch, NexStent®, Medtronic Sprint Fidelis® Defibrillator Leads, and the Zimmer Durom® Cup Hip Replacement.

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