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U.S. Department of Health and Human Services

Class 1 Device Recall HeartMate II System Controller

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 Class 1 Device Recall HeartMate II System Controllersee related information
Date Initiated by FirmMarch 04, 2014
Date PostedMarch 21, 2014
Recall Status1 Terminated 3 on August 27, 2015
Recall NumberZ-1228-2014
Recall Event ID 67639
PMA NumberP060040 
Product Classification Ventricular (assisst) bypass - Product Code DSQ
ProductHeartMate II System Controller Product Usage: HeartMate II is a mechanical device that circulates blood throughout the body when the heart is too weak to pump blood adequately on its own. It is sometimes called a a heart pump or VAD. HeartMate II is a small implantable LVAD. HeartMate II attaches to the heart and is designed to assist or take over the pumping function of the patients left ventricle, the main pumping chamber of the heart.
Code Information Catalog number 106762 (NAm) 106017 - EU all serial numbers
Recalling Firm/
Manufacturer		 Thoratec Corporation
6035 Stoneridge Dr
Pleasanton CA 94588-3270
For Additional Information ContactDonald A. Middlebrook
925-847-8600
Manufacturer Reason
for Recall		Discovery of serious injuries and deaths associated with the process of changing from a primary System controller to their back-up System controller in patients using the Pocket System controller model.
FDA Determined
Cause 2		Device Design
ActionThoratec sent an Urgent Medical Device Correction letter dated March 4, 2014 to all affected customers. The letter was sent via e-mail. All distributors outside of the USA and Canada to whom affected product has been distributed have been notified of this field correction notice and have been provided copies of the Customer Letter to forward to their customers. The letter identified the affected product , problem and actions to be taken. Customers were requested to complete and sign the attached Acknowledgement Form and return it to Thoratec via fax (925-847-8571) or e-mail a scanned copy to customer.service@thoratec.com. For questions call 1-800-528-2577.
Quantity in Commerce4120
DistributionWorldwide distribution: US (nationwide) including states of: AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KY, LA, MA, MD, MI, MN, MO, MS, NC, NE, NJ, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, and WI; and countries of: Austria, Belgium, Czech Republic, France, Germany, Ireland, Israel, Italy, Lebanon, Lithuania, Poland, Saudi Arabia, Singapore, Slovenia, Sweden, Switzerland, The Netherlands, Turkey, and United Kingdom.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
PMA DatabasePMAs with Product Code = DSQ
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