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Recall of HeartMate II LVAS Pocket System Controllers

On March 20, 2017, Abbott-Thoratec issued a recall of 28,882 HeartMate II LVAS Pocket System Controllers following reports of at least 70 malfunctions after patients attempted to exchange controllers while away from the hospital. The FDA recall notice reports that these malfunctions resulted in 19 injuries and 26 deaths. The recalled Model/Item numbers are 105109, 106015, 106762 and 107801, and were distributed between July 2012 and December 2016.

The law firm of Meshbesher and Spence is currently investigating claims involving the recalled Pocket System Controllers. If you or a loved one suffering injury after a malfunction of this device, call us today for a free consultation.

FDA Recall Notice

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With over 50 years of experience representing individuals and families who have suffered injuries or deaths, Meshbesher & Spence's attorneys deliver the very best in individualized service and demonstrated results. You can be assured that you will receive the best legal representation by a law firm known for its integrity and effectiveness. Meshbesher & Spence is your FIRST CALL for personal injury representation. Call now for a free consultation.