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Abbott Recalls HeartMate Touch Communication System for Unintentional Pump Start and Stop

The Abbott HeartMate Touch Communication System is being recalled due to the risk of unintended communication with the HeartMate System Controller resulting in pump stop of the HeartMate 3 Left Ventricular Assist Device.

http://www.fda.gov/medical-devices/medical-device-recalls/abbott-recalls-heartmate-touch-communication-system-unintentional-pump-start-and-stop

 
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Ventec Life Systems Recalls VOCSN Patient Breathing Package (Pediatric, Active, Oxygen, Blue) for Manufacturing Issue with Bonded Spiral Wrap

If the bonded spiral wrap detaches, it can compromise the structural integrity, functionality, or cause blockage, stoppage, or leaks in the breathing circuit.

http://www.fda.gov/medical-devices/medical-device-recalls/ventec-life-systems-recalls-vocsn-patient-breathing-package-pediatric-active-oxygen-blue

 
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Medtronic Neurosurgery Recalls Duet External Drainage and Monitoring System Catheter Tubing due to a Potential for the Catheter Disconnection from the Patient Line Stopcock Connectors

Medtronic Neurosurgery is recalling Duet EDMS catheter tubing due to a potential for disconnection from the patient line stopcock connectors.

http://www.fda.gov/medical-devices/medical-device-recalls/medtronic-neurosurgery-recalls-duet-external-drainage-and-monitoring-system-catheter-tubing-due