Novopen Echo Insulin Device Recall [US]

US/Silver Spring: Novo Nordisk recalls certain batch/lots of Cartridge Holders for Novopen Echo Insulin Delivery Devices due to suspected risk of creaking and/or breakage and consequential Insulin delivery failure, Hyperglycemia and resultant life-threatening complications, all serious health hazards. FDA: http://ht.ly/Aquy30ds3rj

Direct link: https://www.fda.gov/Safety/Recalls/ucm565936.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following medical devices are subject to this recall:

Venture Catheter Recall [US]

US/Silver Spring: Vascular Solutions, Inc. recalls all batch/lots worldwide of Venture Catheters due to suspected extraneous material in the inner lumen of the distal Catheter tip and consequential component detachment or extrusion during use, embolism, serious injury and/or death hazards. FDA: http://ht.ly/Dkzn30d8YmD

Direct link: https://www.fda.gov/Safety/Recalls/ucm564419.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Catheters are subject to this recall (in alphanumeric order):

Wingman35 Crossing Catheter Recall [US]

US/Silver Spring: ReFlow Medical recalls an estimated 2327 Wingman35 Crossing Catheters due to suspected tip splitting and consequential risks of injury, internal laceration and bacterial infection, all serious health hazards. FDA: http://ht.ly/UdCY30bCptV

Direct link: https://www.fda.gov/Safety/Recalls/ucm556525.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Catheters are subject to this recall: