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FDA Recalls Recall Information from the US Food and Drug Administration

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Old 03-23-2012, 12:15 AM
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Default Thoratec Corporation Issues Update on Worldwide Medical Device Correction Notificatio

Thoratec Corporation Issues Update on Worldwide Medical Device Correction Notification Relating to Sealed Outflow Graft Used With HeartMate II Left Ventricular Assist System

On February 23 2012 Thoratec Corporation initiated a voluntary worldwide medical device correction notification of all serial numbers of the HeartMate II Left Ventricular Assist Systems (HM II LVAS) having Catalog No. 104692 103393 104911 or 104912

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