Medtronic Recalls HeartWare HVAD System Batteries Due to Battery Failure
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.
Source: dicardiology.com
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The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.
This is one of multiple recalls that have plagued the device, which was pulled off the market in June 2021.