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Medtronic Recalls Mahurkar Acute Dual Lumen High Flow Hemodialysis Catheters for Potential Catheter Hub Defect

The U.S. Food and Drug Administration (FDA) has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries, serious health consequences, or death ....

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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. ....

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Medtronic Recalls HVAD Pump Implant Kit for Pump Weld Defect

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. ....

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Medtronic Recalls HawkOne Atherectomy System Due to Risk of Tip Damage During Use

Https://www.dicardiology.com/channel/atherectomy-devicesThe FDA has identified this as a Class I recall ....

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