Thoratec Corp Thoratec Dual Drive Console a drive component of the Thoratec Ventricular Assist Device, Model Numbers, 10025-2600-005, 10025-2601-007, 10025-2602-006, Thoratec Corporation, 6035 Stoneridge Drive, Pleasanton, CA 94588 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Thoratec Dual Drive Console a drive component of the Thoratec Ventricular Assist Device, Model Numbers, 10025-2600-005, 10025-2601-007, 10025-2602-006, Thoratec Corporation, 6035 Stoneridge Drive, Pleasanton, CA 94588
Brand
Thoratec Corp
Lot Codes / Batch Numbers
All Dual Drive Consoles manufactured before July 10, 2002 with serial numbers between 301 and 636, inclusive
Products Sold
All Dual Drive Consoles manufactured before July 10, 2002 with serial numbers between 301 and 636, inclusive
Thoratec Corp is recalling Thoratec Dual Drive Console a drive component of the Thoratec Ventricular Assist Device, Model Numbe due to The module power switch (at the back of console) may break while attempting to turn the Dual Drive Console OFF or ON.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The module power switch (at the back of console) may break while attempting to turn the Dual Drive Console OFF or ON.
Recommended Action
Per FDA guidance
The firm issued on 1/25/07 an URGENT: MEDICAL DEVICE CORRECTION-notice informing its consignees about the 'Power Switch Replacement Instructions' and arrangements for their service department replacement of the switches.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026