Brand

Thoratec Corp. Recalls

9 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Thoratec Corp..

9Total Recalls
4Critical
50,203Units Affected
Mar 1, 2024Most Recent
All Recalls

Every Thoratec Corp. Recall

Sorted by most recent. Click any recall for full details.

9 recalls
CriticalFDA
Thoratec Corp.
Thoratec HeartMate 3, LVAS Implant Kit, REF:106524US, Sterile EO, RxOnly
Medical Implants·882 affected·Mar 1, 2024
CriticalFDA
Thoratec Corp.
HeartMate 3 Left Ventricular Assist System (LVAS): 1. HeartMate 3 Sealed Outflow Graft with Bend Relief, Investigational Device Exemptio...
Medical Implants·22,663 affected·Feb 19, 2024
CriticalFDA
Thoratec Corp.
HeartMate II Left Ventricular Assist System (LVAS): 1. HeartMate II Sealed Outflow Graft with Bend Relief REF 103393 2. HeartMate II LV...
Medical Implants·2,240 affected·Feb 19, 2024
CriticalFDA
Thoratec Corp.
1. HeartMate Touch Communication System, REF HMT1100 2. HeartMate Touch Communication System, Rental REF HMT1100-R 3. HeartMate Touch C...
Cardiac Devices·1,560 affected·Jan 3, 2024
High RiskFDA
Thoratec Corp.
Abbott HeartMate Touch Communication System, REF: HMT1100 (US), HMT1100-R (Rental US), HMT1150 (EU)
Cardiac Devices·988 affected·Oct 22, 2021
High RiskFDA
Thoratec Corp.
HeartMate 3 Mobile Power Unit, REF 107754, UDI or GTIN: 00813024010883, and 107758, UDI or GTIN: 00813024010890, when connected to the He...
Cardiac Devices·13,871 affected·Dec 2, 2019
High RiskFDA
Thoratec Corp.
Thoratec Heartmate 3 Sealed Outflow Graft with Bend Relief, Sterile, REF 105581US/105581, RX only, Part of Left Ventricular Assist Device...
Cardiac Devices·149 affected·Mar 30, 2019
High RiskFDA
Thoratec Corp.
Thoratec HeartMate 3 LVAS Implant Kit, Sterile, REF 106524/106524US, RX only, Left Ventricular Assist System
Medical Implants·7,200 affected·Mar 30, 2019
High RiskFDA
Thoratec Corp.
Thoratec HeartMate 3 Coring Tool, Sterile EO, Rx Only, REF 10005872, an optional accessory of Thoratec HeartMate 3 Left Ventricular Assi...
Cardiac Devices·650 affected·Mar 1, 2019