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Open, Classified

HeartWare Ventricular Assist Device (HVAD) System Batteries, Product Number 1650DE

FDA Recall Z-1512-2022 · Posted 2022-08-18

Recalling FirmHeartware, Inc.
Recall StatusOpen, Classified
Product CodeDSQ
Date Initiated2022-06-28
Product Quantity19616 batteries

Reason for Recall

Battery performance issues. Battery electrical faults render it unable to power the controller, unable to accept charge from the battery charger, and/or result in the battery to appear to remain charged while discharging.

Firm Action

Medtronic (Heartware) issued a Medical Device Correction notice on 06/28/2022 by letter. The notice, addressed to the VAD Coordinators, explained the issues and provided the following recommendations: 1. Please remind your patients to always keep two sources of power connected to their controller and have fully charged spare batteries available at all times. 2. Remind patients to acknowledge and report alarms. 3. Follow the Instructions for Use (IFU) for proper power source management. 4. Inform patients to be vigilant if the battery indicator lights do not decrease over time while the battery is in use. Customer Actions: Complete the enclosed Customer Confirmation Form please return the form to [email protected]. Please share this letter with all those who need to be aware within your organization or to any organization where patients have been transferred. UPDATE: Medtronic/Heartware issued an Urgent Medical Device notice to its consignees on 05/31/2023 via UPS 2nd day delivery. The notice is a follow-up to Medtronic's existing June 2022 customer notification letter titled "Urgent Medical Device Correction". The notice explained the issue, risk, and announced that Medtronic will begin all batteries for the new batteries with the change to the battery configuration mode. For questions regarding this communication, please contact your local Medtronic Field Representative. Medtronic Patient Services is available to assist patients at 800-635-3930 (Monday-Friday, 8 a.m.-5 p.m. Central Time). For any additional questions you can reach out to the Medtronic Office of Medical Affairs at [email protected].

Root Cause

Device Design

Distribution Pattern

Worldwide distribution. US nationwide, Japan, Indonesia, Brazil, Chile, Belgium, Italy, Germany, Switzerland, United Kingdom, Poland, Hungary, Czech Republic, Mauritius, France, South Africa, Greece, Netherlands, Sweden, Norway, Denmark, Estonia, Lebanon, Croatia, Spain, Austria, United Arab Emirates, Luxembourg, Canada, Korea, Republic Of, Israel, Qatar, India, Australia, New Zealand, Taiwan, Malaysia, Hong Kong, Singapore, Latvia, Saudi Arabia, Slovakia, North Macedonia, Finland, Turkey, Armenia, Colombia, Kazakhstan, Kuwait, Serbia, Bahrain, Egypt, Pakistan, and Ukraine.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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