Philips Recalls BrightView Imaging Systems Due to the Detector Unexpectedly Falling
Please be aware, this recall is a correction, not a product removal.
Source: itnonline.com
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Abiomed Recalls the Labeling for Impella RP Flex with SmartAssist for Risk of Blood Clots
Abiomed is recalling the labeling for Impella RP Flex with Smart Assist System Catheter because the catheters’ Instructions for Use (IFU) do not appropriately address precautions for healthcare providers to take when treating patients whose anticoagulation clotting time is below the recommended value
Source: dicardiology.com
Teleflex and Arrow International Recall ARROW Endurance Extended Dwell Peripheral Catheter System
Teleflex and Arrow International recall ARROW Endurance Extended Dwell peripheral catheter system due to risk of catheter separation and leakage
Source: dicardiology.com
Abiomed Recalls Specific Impella 5.5 with SmartAssist for Purge Fluid Leaks that Can Cause Pump Stop and Loss of Support
According to a news release issued by the U.S. Food and Drug Administration (FDA), Abiomed has recalled specific Impella 5.5 with SmartAssist for purge fluid leaks that can cause pump stop and loss of support. 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
Teleflex Recalls Arrow Intra-Aortic Balloon Pumps for Short Battery
Arrow International, LLC, a Subsidiary of Teleflex, Inc, recalls Arrow AutoCAT 2, AC3 intra-aortic balloon pumps for unexpectedly short battery run times
Source: dicardiology.com