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Device Lookup

For HeartMate 3 LVAS System Controller Medical Device Correction

In July 2024, Abbott is notifying customers of a potential issue identified with HeartMate 3™ System Controllers. Abbott has identified that there is a potential for specific controllers to have a lifted User Interface (UI) membrane that when present, is observed along the edge of the controller housing, near the Display Button. The product is not being removed from the field.

This tool enables healthcare professionals to confirm if a specific device is subject to this safety notification.

Check for a Device

 

Please enter a correct model number Please enter a correct model number Please enter a correct model number
Please enter a correct serial number Please enter a correct serial number Please enter a correct serial number

Device Lookup Instructions

Please follow the steps below to determine if a HeartMate 3 Controller is subject to this notification.

  1. Enter the device model and controller serial number above; both are required.
  2. If the device is subject to this notification, review the recommendations in the safety notification.
  3. If the device is not subject to this notification, no further action related to this notification is needed.

If you are a patient and have questions about your device, please contact your treating physician.

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Information contained herein for distribution outside the U.S. only.

CAUTION: These products are intended for use by or under the direction of a physician. Prior to use, reference the Instructions for Use, inside the product carton (when available) or online for more detailed information on Indications, Contraindications, Warnings, Precautions and Adverse Events.

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