Sep 2, 2016 | Defective Medical Devices, Defective Products, Personal Injury, Product Liability, Recalled Products
CareFusion has recalled the AVEA Ventilator, which the FDA has identified as a Class I recall. This is the most serious class of recalls because using the device can result in serious injury or even death. Several components have been recalled related to this product:...
Jun 22, 2016 | Defective Medical Devices, Defective Products, Personal Injury, Recalled Products
The FDA has identified the recall of battery packs used with the Capnostream™ 20 and Capnostream™ 20p Patient Monitors as a Class I recall. A Class I recall is the most serious type of recall. Using the batteries can cause serious injury or death. Medtronic...
