Thoratec recalls HeartMate Touch Communication System models HMT1100 and HMT1150 due to software and controller systems causing unexpected pump start or stop. Affected units have specific serial numbers listed in the recall notice.
Due to software and controller systems that results in unexpected pump start or pump stop.
Thoratec is recalling HeartMate Touch Communication Systems with model numbers HMT1100 and HMT1150 because software and controller issues can cause the device to start or stop unexpectedly. This poses a risk for patients using left ventricular assist devices.
The software and controller systems in these devices can cause unexpected pump start or stop events. This may lead to complications for patients relying on the left ventricular assist device for heart support.
Patients using HeartMate 3 Left Ventricular Assist Systems (LVAS) with the HeartMate Touch Communication System are most at risk. The recall affects specific model numbers and serial numbers listed in the notice.
Check if your HeartMate Touch Communication System has model number HMT1100 or HMT1150 with the serial numbers listed in the recall notice. The device is used with HeartMate 3 LVAS systems.
Identify if your HeartMate Touch Communication System has model number HMT1100 or HMT1150.
If your device is listed in the recall, contact Thoratec for further instructions.
The HeartMate Touch Communication System is a software application loaded onto a tablet that provides a user interface for programming and monitoring HeartMate 3 Left Ventricular Assist Systems (LVAS).
Check if your HeartMate Touch Communication System has model number HMT1100 or HMT1150 with the specific serial numbers listed in the recall notice.
No, but you should check if your device is listed in the recall and contact Thoratec for further instructions.
We’ve drafted a message you can send Thoratec Corp. to request your refund or repair — edit it as you like.
Subject: Recall Z-0842-2024 — Thoratec Corp. Thoratec Corp. Hello, I own a Thoratec Corp. that is covered by recall Z-0842-2024 from Thoratec Corp.. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
