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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Class I Recall of Percutaneous Thrombolytic Device
Arrow-Trerotola over-the-wire 7FR PTD kits are being recalled because the orange inner lumen of the catheter's tip may separate from the basket causing injury.
Source: medscape.com