Thoratec Corp. Abbott HeartMate Touch Communication System, REF: HMT1100 (US), HMT1100-R (Rental US), HMT1150 (EU) Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Abbott HeartMate Touch Communication System, REF: HMT1100 (US), HMT1100-R (Rental US), HMT1150 (EU)
Brand
Thoratec Corp.
Lot Codes / Batch Numbers
All serial numbers.
Products Sold
All serial numbers.
Thoratec Corp. is recalling Abbott HeartMate Touch Communication System, REF: HMT1100 (US), HMT1100-R (Rental US), HMT1150 (EU) due to If LVAS communication system is trying to establish Bluetooth connection and another Bluetooth-enabled device is nearby and advertising for Bluetooth . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
If LVAS communication system is trying to establish Bluetooth connection and another Bluetooth-enabled device is nearby and advertising for Bluetooth connection, the Bluetooth connectivity interference may cause the system App to close or fail to open. Once Bluetooth adaptor is connected, barring disconnection, all functionality is unaffected; the device will continue to operate as expected.
Recommended Action
Per FDA guidance
On 10/22/21, correction notices were provided via site visit, or email. Until the resolution is provided, the recalling firm is requesting that your facility retain or obtain the System Monitor II (Model Numbers 1286 and L1286) and ensure it is readily available for use in the event that the LVAS communication system is unable to function properly. The recalling firm is extending the support and servicing of System Monitors II until this issue is resolved and the resolution is fully implemented in the field. If your facility does not have a System Monitor II, the recalling firm will provide a loaner System Monitor II at no charge until a corrective action is provided to your facility. If your facility has not previously used a System Monitor II, the recalling firm will provide training and implementation support to your facility. A firm representative will work with you to schedule a time that is convenient for you and your staff. If you have any questions about this communication or the recommendations, please contact your local representative or Technical Support at 1-800-456-1477 (U.S.). Please share this notice with all those within your organization who might operate the affected device. We ask that you maintain a record of this notice to ensure effectiveness of the communication. Please complete and return the response form.
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