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FDA Medical Device Recalls (openFDA)

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 number
Z-0412-2007
Recalling firm
Thoratec Corp
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
Status
Terminated
Initiated
2004-09-24
Posted
2007-02-10
Terminated
2008-04-18
Reason
The module power switch (at the back of console) may break while attempting to turn the Dual Drive Console OFF or ON.
Root cause
Other
Action
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.
Quantity
331
Distribution
Worldwide
Lot, serial or model codes
All Dual Drive Consoles manufactured before July 10, 2002 with serial numbers between 301 and 636, inclusive
510(k) numbers
not on file
PMA numbers
["P870072"]
Product code
DSQ
Firm FEI
2916596
Firm city
Pleasanton
Firm state
CA
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

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Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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