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U.S. Department of Health and Human Services

Class 1 Device Recall HeartMate II Implant Kit with Pocket Controller;

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  Class 1 Device Recall HeartMate II Implant Kit with Pocket Controller; see related information
Date Initiated by Firm March 04, 2014
Date Posting Updated March 21, 2014
Recall Status1 Terminated 3 on August 27, 2015
Recall Number Z-1227-2014
Recall Event ID 67639
PMA Number P060040 
Product Classification Ventricular (assisst) bypass - Product Code DSQ
Product HeartMate II Implant Kit with Pocket Controller;
with sealed grafts (NAm)
with sealed grafts (EU)

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.
Code Information Catalog number 106015 (NAm), 106016 - EU, all serial numbers
Recalling Firm/
Thoratec Corporation
6035 Stoneridge Dr
Pleasanton CA 94588-3270
For Additional Information Contact Donald A. Middlebrook
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
Action Thoratec 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 Commerce 1737 catalog number 106015; 609 catalog number 106016
Distribution Worldwide 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 Cycle TPLC 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 Database PMAs with Product Code = DSQ and Original Applicant = THORATEC CORP.